INTERNATIONAL PROTECTION OF PATENT WITH SPECIAL REFERENCE TO TRIPs AGREEMENT.
INTRODUCTION
Intellectual
property is an area of the world’s numerous attributes that cannot be ruled
out. This owes to the established fact that every day, somewhere and in some time,
the human mind goes on thinking and conceiving ideas that could better the
peaceful sustenance of humanity. International business has increased
tremendously over the past few years. Internet use has allowed people to access
information from all over the globe. Luckily, many nations have formed
international laws that provide global protection for all intellectual property.
Intellectual
Property (IP) has been traditionally categorized into Industrial property and
Copyright. The term Industrial Property includes patents, trademarks,
industrial designs, and geographic indications of source. Copyright protection
is granted to protect literary, artistic and musical works. Rights related to
copyright include those of performing artists in their performances, producers
of phonograms in their recordings, and those of broadcasters in their radio and
television programs. Intellectual property rights are generally said
to be a bundle of exclusive rights granted to the lawful owner.
The
term intellectual property denotes the specific legal rights, and not the
intellectual work itself. It is important to be aware of what these IP rights
are, how they can be protected and, in due course, how to benefit from them.
The
protection of IPR has been an international issue since the second half of the
19th century and the variety of business transactions that are
increasingly adding up in numbers can only be secured by a very stable and
comprehensive IPR system, though, we consider a world economy with on-going
innovation in two countries that differ in market size, in their capacities for
innovation, and in their absolute and comparative advantage in manufacturing.
WHAT IS PATENT?
Patent
is a form of protection that provides a person or legal entity with exclusive
rights for making, using or selling a concept or invention and excludes others
from doing the same, also for claiming damages from those who infringe the
invention.
A
patent is also an exclusive right granted by rhe government to a patentee for a
fixed period of time in exchange for the regulated public disclosure of certain
details of a device, method, process, or composition of matter known as an
invention which is new, inventive and useful.[1]
Patents
generally cover innovations, products or processes that include new functional
or technical aspects. It is granted by the Indian Patent Office and has a term
of 20 years. After expiration of this 20 year monopoly the product/ invention
will fall in the public domain for any third party to use it.
The
legislations which deal with the protection and registration of patents in
India are The Patent Act, 1970 and The Patent Rules 2003. The patent Act 1970
has undergone three (3) amendments in 1999, 2002 and 2005. In the 2005
amendment introduced product patent protection for food, pharmacueticals and
chemical inventions.
In
India an invention/product has to satisfy various criteria to qualify for a
patent are:
- New/
Novel- The invention has a feature that sets it
apart from previous inventions and is unknown to the public.
- Non-obviousness-
The invention’s novelty must not be obvious to someone who has ordinary
skill in the area of invention.
- Utility-
The invention is considered useful[2].
INTERNATIONAL PROTECTION OF PATENTS
The
important agreements that should be considered when contemplating international
patent protection are:
A.
Paris Convention 1883
B.
The General Agreement on Tariffs and
Trade (GATT)
C. World
Trade Organisation (WTO)- Trade Related Aspects of
Intellectual Property Rights (TRIPS).
D.
World Intellectual Property Organisation
(WIPO)
E.
Patent Coperation Treaty (PCT)
F.
Patent Law Ttreaty (PLT).
THE PARIS CONVENTION OF 1883
The
Paris Convention is basically for the protection of Industrial property. It is
one of the first and the most important multilateral treaties protecting
intellectual property. Due to the difficulty in obtaining protection in various
countries because of diversity of laws and publication in one country
destroying novelty in another, a strong desire to overcome them arose and thus,
led to the conference in Paris on March 20, 1883, which ended with final
approval and signature of Paris convention for the protection of industrial
property and it became effective on March 7, 1884.[3]
The
Paris Convention was conceived to eliminate the threat of an inventor's work
being stolen and used in another country where they would be free of any
national patent laws protecting the invention. Inventors from around the world
were reluctant to attend world fairs to display their new strides in
technology.
This
convention terms has been revised at Brussels on December 14, 1900, at
Washington on June 2, 1911, at The Hague on November 6, 1925, at London on June
2, 1934, at Lisbon on October 31, 1958, at Stockholm on July 14, 1967 and as
amended on September 28, 1979.[4]
It
was intended to apply to only Industrial properties in a very broad sense like patents,
utility models, industrial designs, trademarks, service marks, trade names,
indications of source or appellations of origin, and the repression of unfair
competition.
·
Article 1(3) of Paris Convention states
that Industrial
property shall be understood in the broadest sense and shall apply not only to
industry and commerce proper, but likewise to agricultural and extractive
industries and to all manufactured or natural products, for example, wines,
grain, tobacco leaf, fruit, cattle, minerals, mineral waters, beer, flowers,
and flour.
·
Article 1(4) states that Patents shall
include the various kinds of industrial patents recognized by the laws of the
countries of the Union, such as patents of importation, patents of improvement,
patents and certificates of addition, etc.
MAIN PRINCIPLES OF PARIS CONVENTION
A. PRINCIPLE OF NATIONAL
TREATMENT.
Article
2 of the convention stipulates that states should not subject foreigners to
higher protection standards than those applicable to its citizens. This
principle first applies to nationals of member countries, both natural and legal
persons, and then to nationals of non-member countries, if they are domiciled
or have an industrial or commercial establishment in a member country. An
exception to this rule is that states can refuse protection to non-member
countries as it wills.
B. PRINCIPLE OF RIGHT OF PRIORITY
The
right of priority means that, on the basis of regular application for
industrial property right filed by a given applicant in one of the member
countries, the same applicant or his successor in title may, within a specified
period of time, apply for protection in all other member countries. These later
applications will be regarded as if they were filed on the same day as the
earliest application. They enjoy a priority status in respect to all
applications on same invention.
C. INDEPENDENCE OF PATENTS.
This
implies that patents granted for inventions in member countries to nationals or
its residents should and must be treated as independent of patents for
invention obtained for the same invention in other countries, including
non-member countries. It clearly implies that the grant of patent by one
country does not impose on any other country to grant patent for the same
invention. More on that, granting of patent cannot be refused by any member
country on the ground that a patent for the same invention has been refused by
another country.
COMMON RULES FOR PATENT
Among
the Convention provisions that provide substantive rules protecting patents and
patentees are the following:
A. The Principle of Independence of
Patents: Embodied in Article (4b) the principle that a patent
application in one country of the Union is examined and granted or denied
independent of applications for patents for the same or related inventions
filed in other countries within and without the Union. Also, according to
Article (4b) and (5), patent terms are measured in accordance with the
applicable national law without regard to (not shortened by) a priority claim.[5]
B. Right of the Inventor to be
Mentioned: Article 4ter provides that the “inventor has the
right to be named as such in the patent.”[6]
C. Patentability not Effected by
Restrictions on the Product: Article 4quarter provides that a
patent shall not be refused or invalidated because the product patented or
obtained by means of a patented process is subject to restrictions on its sale
or importation under the domestic law.[7]
D. Importation of Patented Products or
Products Made from Patented Processes: Article 5A(1)
provides that importation into a member country of products for which a patent
has been granted in that country manufactured in another member country cannot
result in forfeiture of patent rights in the country of importation.[8]
Article
5quarter provides that with respect to products imported into a member country
manufactured by a process patented in the country of importation, the patentee
will have all the rights with respect to the imported product that would
normally be accorded the patentee with respect to products manufactured in that
country. This latter provision protects the patentee of a process from
importation into the country of finished products manufactured by the patented
process outside the country of importation, but only where the domestic patent
laws of the country of importation extend the patent right to products
manufactured by patented processes.
E. Failure to Work and Compulsory
Licenses: Article 5A(2) through (4) allows countries to
enact protectionist legislative measures granting compulsory licenses in order
to prevent abuses that might result from the exclusive rights conferred by a
patent for invention, namely the failure to work or to work sufficiently the
patented invention within the member country, but the failure to work an
invention cannot result in forfeiture of the patent except in cases where the
grant of a compulsory license would not have been sufficient to prevent the
abuse, and then only pursuant to a proceeding instituted no sooner than two
years following the grant of the first compulsory license. Compulsory licenses
must be non-exclusive, and cannot be granted before the later of four years
from the date of filing of the patent application or three years from the grant
of the patent. Compulsory licenses may also be granted in special cases,
without alleged abuse on the part of the patent owner, where the patent affects
a vital public interest, for example, in the fields of defense or public
health. Compare Article 27 of TRIPS prohibiting countries from adopting working
requirements for patents.
F. Grace Period for Maintenance Fees:
Article 5bis guarantees those holding patents in member states a grace period
of at least six months to pay prescribed maintenance fees, and allows member
states to provide for the restoration of patents that have lapsed by reason of
non-payment of maintenance fees.
G. Patents in International Traffic:
According to Article 5ter, patented devices on board ships, aircraft or land
vehicles of other member countries that enter temporarily or accidentally
within the territory of another member country need not obtain the approval or
license from the patent owner by virtue of the temporary or accidental
intrusion.
H. Inventions Shown and Marks
Exhibited at International Exhibitions: According to Article
11 of the Convention, member countries are obliged to grant temporary
protection, in the form of a right of priority or other assurance against the
destruction of novelty, to inventions, models, designs and marks in respect of
goods exhibited at “official” or “officially recognized” international
exhibitions held in the territory of a member country.
GENERAL AND
ADMINISTRATIVE PROVISIONS
Article 12
of the Convention obligates member states to establish a central industrial
property service, either itself or through a regional organization, responsible
for communicating with the public on matters of patents, trademarks and the
like, which service must also publish an official periodical journal.
Article 19
of the Convention specifically permits member countries to conclude separate
agreements among themselves for the protection of industrial property as long
as these separate agreements do not include provisions that contravene those of
the Paris Convention.
Article 28
provides that disputes not otherwise settled may be brought before the
International Court of Justice, but parties adhering to the Convention may, at
the time of accession, opt out of this provision.
Other
administrative provisions provide for the governmental organs of the Union,
comprising an Assembly composed of
representatives from each member nation that meets every two years and
formulates long term policy and direction; an Executive Committee composed of one fourth of the membership of the
Union, that meets once yearly; and the
International Bureau, headed by the Director General of WIPO, that handles
the day to day administrative tasks of the Union.[9]
The
recent TRIPs agreement accords so much significance to the Paris convention for
its complexity and uniqueness. The question of universal protection was sought
to be rectified by this convention. 1t goes beyond a mere treaty establishing
rights and obligations to establishing a legal entity to carry out certain
tasks.
It
also benefited inventors by allowing them access for their work into foreign
markets. In addition, the Paris Convention has become one of the largest
international treaties in the world, enlisting 173 countries under its
guidelines. This is a testament to its importance in intellectual property to
protect the natural right to have exclusive rights to one's own work and for
the growth of new ideas through inspiration.
GENERAL AGREEMENT ON TARIFFS AND
TRADE (GATT) 1948
From
1948 to 1994, the General Agreement on Tariffs and Trade (GATT) provided the
rules for much of world trade and presided over periods that saw some of the
highest growth rates in international commerce. It seemed well-established, but
throughout those 47 years, it was a provisional agreement and organization.
The
original intention was to create a third institution to handle the trade side
of international economic cooperation, joining the two “Bretton Woods”
institutions, the World Bank and the International Monetary Fund. Over 50
countries participated in negotiations to create an International Trade
Organization (ITO) as a specialized agency of the United Nations. The draft ITO
Charter was ambitious. It extended beyond world trade disciplines, to include
rules on employment, commodity agreements, restrictive business practices,
international investment, and services. The aim was to create the ITO at a UN
Conference on Trade and Employment in Havana, Cuba in 1947.
Meanwhile,
15 countries had begun talks in December 1945 to reduce and bind customs
tariffs. With the Second World War only recently ended, they wanted to give an
early boost to trade liberalization, and to begin to correct the legacy of
protectionist measures which remained in place from the early 1930s.
This
first round of negotiations resulted in a package of trade rules and 45,000
tariff concessions affecting $10 billion of trade, about one fifth of the
world’s total. The group had expanded to 23 by the time the deal was signed on
30 October 1947. The tariff concessions came into effect by 30 June 1948
through a “Protocol of Provisional Application”. And so the new General
Agreement on Tariffs and Trade was born, with 23 founding members (officially
“contracting parties”).
For
almost half a century, the GATT’s basic legal principles remained much as they
were in 1948. There were additions in the form of a section on development
added in the 1960s and “plurilateral” agreements (i.e. with voluntary
membership) in the 1970s, and efforts to reduce tariffs further continued. Much
of this was achieved through a series of multilateral negotiations known as
“trade rounds” — the biggest leaps forward in international trade
liberalization have come through these rounds which were held under GATT’s auspices.
In
the early years, the GATT trade rounds concentrated on further reducing
tariffs. Then, the Kennedy Round in the mid-sixties brought about a GATT
Anti-Dumping Agreement and a section on development. The Tokyo Round during the
seventies was the first major attempt to tackle trade barriers that do not take
the form of tariffs, and to improve the system. The eighth, the Uruguay Round
of 1986-94, was the last and most extensive of all. It led to the WTO and a new
set of agreements.[10] GATT dealt with only goods but not services
and this was its only problem.
In
India, it effected the changing of MRTP Act to Competition Act and in 1995,
GATT changed to World Trade Organisation (WTO).
THE OBJECTIVE OF GATT
A.
Reducing barriers for international
trade.
B.
Raising standard of living.
C. To
expand production.
D. To
utilise the world wide resources.
E. To
ensure employment.
F. Reduction
of tariff and other trade barriers.
G. Discuss
and resolve their trade disputes and discuss to enlarge world trading
opportunities.[11]
BASIC PRINCIPLES OF GATT
A.
No discrimination
·
National treatment
·
Most Favoured Nation Treatment
B. Predictability
·
Through binding
·
Transparency
C. Freer
trade that is suppression of trade obstacles through negotiations.
D. Encourage
development.
WORLD TRADE ORGANISATION
(WTO) 1994 – TRADE RELATED ASPECTS OF INTELLECTUAL PROPERTY RIGHTS (TRIPs).
TRIPs
is an international agreement administered by WTO, which sets standards for
intellectual property. It was negotiated at the end of Uruguay round of the
general agreement on tariff and trade in 1994. The agreement lays down general
principles applicable to Intellectual property and came into force on 15th
January 1995. It is also the most comprehensive multilateral agreement on
Intellectual Property.
TRIPS
consist of 7 intellectual property items namely:
a.
Copyright and other related rights.
b.
Trademark.
c.
Industrial designs.
d.
Geographical Indications.
e.
Patents.
f.
Integrated circuits..
g.
Undisclosed information.
The
Uruguay Round achieved that. The WTO’s TRIPS Agreement is an attempt to narrow
the gaps in the way these rights are protected around the world, and to bring
them under common international rules. It establishes minimum levels of
protection that each government has to give to the intellectual property of
fellow WTO members. In doing so, it strikes a balance between the long term
benefits and possible short term costs to society. Society benefits in the long
term when intellectual property protection encourages creation and invention,
especially when the period of protection expires and the creations and
inventions enter the public domain. Governments are allowed to reduce any short
term costs through various exceptions, for example to tackle public health
problems. And, when there are trade disputes over intellectual property rights,
the WTO’s dispute settlement system is now available.
The
agreement covers five broad issues:
·
How basic principles
of the trading system and other international intellectual property agreements
should be applied.
·
How to give adequate
protection to intellectual property rights.
·
How countries should
enforce those rights adequately in their own territories.
·
How to settle disputes
on intellectual property between members of the WTO.
·
Special transitional
arrangements during the period when the new system is being introduced.[12]
PRINCIPLES OF TRIPs
A.
NATIONAL TREATMENT.
It strengthens the principle of national
treatment as it was first incorporated in Paris convention. It entails that
each member of WTO shall accord to the nationals of other members a treatment
which is not less favourable as it would give to her own member nationals with
respect to the protection on Intellectual property. The national treatment
charge in TRIPs differs from that which existed under Article III of GATT 1994.
GATT addresses trade in goods the non-discriminatory implication is in respect
to products or tangible things while in TRIPs, it is in relation to
non-discrimination to persons. In a nutshell, it is treating one’s own
nationals and foreigners equally. When legal rules distinguish in their
express between foreign and local nationals, this may constitute discrimination
as a matter of law, of dejure discrimination. One the other hand, legal rules
that use identical terms to address foreign and local nationals may appear
neutral, but in fact produce discriminatory results through operation in
practice. When finally natural legal rules are discriminatory in effect, this
is referred to as dejure discrimination. The TRIPs
agreement includes both dejure and defacto discriminations.[13]
B.
MOST FAVOURED NATION PRINCIPLE (MFN)
The MFN principle was not specifically
included in the WIPO convention since it was assumed that its members would not
grant intellectual property rights to foreign nationals to a larger extent that
their own nationals. This had to change when in the late 1980’s, bilateral
pressures was mounted to increase IPR protection. Uruguay round negotiators
became concerned that some countries even granted protection to foreign
nationals than their own nationals and thus led to incorporating MFN into
TRIPs.
MFN requires that each member should treat
national of all other members on an equal basis in relation to Intellectual Property.
The working of this principle will increase the allocation of resources and
thereby lowering the cost of production, increasing the number of consumer
choices and promoting world economic growth. It will also facilitate trade
negotiations.
C.
The TRIPS Agreement
has an additional important principle:
intellectual property protection should contribute to technical innovation and
the transfer of technology. Both producers and users should benefit, and
economic and social welfare should be enhanced, the agreement says.
EXHAUSTION OF
INTELLECTUAL PROPERTY RIGHTS UNDER TRIPs
Due to divergence
between negotiating states, no consensus could be found on the question
of exhaustion. The issue is whether the first introduction of a patented
product in the market by the patent owner or with the patent owner’s consent
exhausts the rights that can be claimed on the basis of the relevant patent?
Two main points can be highlighted:
Firstly, there is the question whether the
introduction of patented product in one country exhausts the right in all
countries where the product is patented or only in the country where it is
introduced. This has been especially contentious in the case of medical patents
because of the links between exhaustion, parallel imports and differential
pricing. In the case of national exhaustion, there is scope for companies that
wish to do so to sell their drugs at different prices in different markets
taking into account different levels of economic development and capacity to
pay.[14]
In the case of drugs for diseases that exist both in developed and developing
countries; differential pricing can have positive aspects. It allows
pharmaceutical companies to sell in developed countries at a level, which
allows them to maintain their profit levels. At the same time, the segmentation
of the market permits the sale to developing countries of the same drug at a
price much closer to the marginal cost of production may still be much more
than what most patients in developing countries can afford. Similarly even if
the price of a single dose is ‘affordable’ this may not be the case if a drug
is to be taken for a long period of time.[15]
Secondly,
differential pricing does not solve the problem of the incentive to the private
sector pharmaceutical industry in the case of diseases, which occur only in
developing countries. The prices that developing countries can afford are not
sufficient to entice a developed country company to engage in the necessary
research and development.[16]
Thirdly, there is
the issue of the actual meaning of exhaustion in specific cases.
Article 6 of the
TRIPs agreement does not provide a general solution to the question of
exhaustion.
COMMON RULES OF TRIPs ON PATENT
a.
The
agreement says patent protection must be available for inventions for at least
20 years.
b.
Scope of patent. General
principles concerning the scope of patentability establish the widest possible
scope. Some optional exceptions have, however, been introduced, allowing member
states to take measures at the national level to retract patentability in
certain specific fields.[17]
c.
Patent
protection must be available for both products and processes, in almost all
fields of technology.
d.
Governments
can refuse to issue a patent for an invention if its commercial exploitation is
prohibited for reasons of public order or morality.[18]
e.
They
can also exclude diagnostic, therapeutic and surgical methods, plants and
animals (other than microorganisms), and biological processes for the
production of plants or animals (other than microbiological processes).[19]
f.
Plant varieties, however,
must be protectable by patents or by a special system (Such as the breeder’s
rights provided in the conventions of UPOV — the International Union for the Protection of New
Varieties of Plants).
g.
RIGHTS OF PATENTEE. The agreement describes the minimum
rights that a patent owner must enjoy like the patent holder has exclusive
rights to prevent third parties from making, using, offering for sale, selling
or importing for these purposes the patented product without the consent of
owner but it also allows certain exceptions. A patent owner could abuse his
rights, for example by failing to supply the product on the market.[20]
Where the patent is for a process, the rights granted extend to the use of the
process and also to the use, sale and import of products that are directly
obtained through the protected process.[21]
These exclusive rights which is obviously monopoly is given 20 years
protection.
Article 30 of the TRIPs provides that;
limited exception to the exclusive rights conferred by a patent provides that
such exceptions do not unreasonably conflict with a normal exploitation of the
patent and do not unreasonably prejudice the legitimate interest of the patent
owner, taking account of the legitimate interests of third parties. This
clause, which only operates at the level of the regulation of the use of a
patent already granted is potentially wide ranging because there is no
definition of the limited exceptions that are allowed.
Member states should thus be able to use
Article 30 to justify a variety of socio-economic measures they may wish to
take to control the abuse of patent rights. But the exception must not
unreasonably conflict with the exploitation of the patent, and thirdly the
exceptions should not unreasonably prejudice the legitimate interests of the
patent owner. However, the structure of Article 30 seems to imply that the
legitimate interests of third parties are subordinate to the interests of
patent holders.
Even if this is the case, there are
situations such as the case of life saving patented drugs where the legitimate
interests of third parties, such as people suffering from HIV/AIDS, could be
deemed to override other interests and allow states to adopt exceptions.
h.
The agreement says governments can issue “compulsory licences”, allowing a
competitor to produce the product or use the process under licence. But this
can only be done under certain conditions aimed at safeguarding the legitimate
interests of the patent-holder.
Article
31 provides a number of conditions that states must follow. These include:
(i) compulsory licensing can only be allowed on a case-to-case basis.[22]
(ii) States must first try to secure
authorization on commercial terms unless it is a situation of national
emergency or the state wants to make public non-commercial of the invention.
(iii) The term of the licence must be
limited in time to the purpose for which it is authorized, must be
non-exclusive, and must be mainly to supply the domestic market.
(iv) The patent holder is entitled to
‘adequate’ remuneration.
One of the interesting features of the
compulsory licensing regime under TRIPs is that there is no limitation of the
purpose for which compulsory licenses can be granted. This can be read as gain
for developing countries since the United States wanted to restrict the grounds
for compulsory licenses. Further states are also free to determine what
constitutes a national emergency.[23]
i.
If a patent is issued for a production process, then
the rights must extend to the product directly obtained from the process. Under
certain conditions alleged infringers may be ordered by a court to prove that
they have not used the patented process.[24]
j.
Temporary exceptions were also granted. Such exception
allowed developing countries like India to retain specific exclusions to
product patentability for ten years after the entry in to force of TRIPs
agreement. This covered, for instance, the product patents for pharmaceutical,
which did not have to be introduced before January 2005.
Some conditions were, however, attached to
this exclusion. Firstly the extra time could not be used to change laws in a
way that would have taken the country further away from compliance, for
instance by introducing further restrictions on patentability during the
transitional period.[25]
Secondly, in the case of restrictions on pharmaceutical and agricultural
products, countries had to introduce a means for filling applications for
patents on such invention.[26]
Further in the intervening period, patent applications were to be granted.
k.
Exclusive Marketing Rights (EMRs) for a period of 5
years or until the acceptance or rejection of the application.[27]
An issue that has arisen recently is how to ensure patent protection for
pharmaceutical products does not prevent people in poor countries from having
access to medicines — while at the same time maintaining the patent system’s
role in providing incentives for research and development into new medicines.
Flexibilities such as compulsory licensing are written into the TRIPS
Agreement, but some governments were unsure of how these would be interpreted,
and how far their right to use them would be respected.
A large part of this was settled when WTO ministers issued a special
declaration at the Doha Ministerial Conference in November 2001. They agreed
that the TRIPS Agreement does not and should not prevent members from taking
measures to protect public health (Article 8). They underscored countries’
ability to use the flexibilities that are built into the TRIPS Agreement. And
they agreed to extend exemptions on pharmaceutical patent protection for
least-developed countries until 2016. On one remaining question, they assigned
further work to the TRIPS Council — to sort out how to provide extra
flexibility, so that countries unable to produce pharmaceuticals domestically
can import patented drugs made under compulsory licensing. A waiver providing
this flexibility was agreed on 30 August 2003.[28]
Article 7 is the only provision, which evokes the balance between the
rights granted to individual intellectual property rights holders and the
broader interests of society at large. In the TRIPs context, the focus is on
the use of intellectual property rights as incentives for foreign investment
and technology transfer.[29]
EFFECT OF TRIPs ON INDIAN PATENT LAWS
India became signatory to the Agreement on Trade Related aspects of
Intellectual Property Rights (TRIPs) of the World Trade Organization in 1995
along with other developing countries with a hope that TRIPs regime will result
in free flow of trade, investment and technical know- how among the member
countries by removing barriers that exists in the form of differences in the
standards of intellectual property.
TRIPS AGREEMENT AND AMENDMENTS TO
THE INDIAN PATENTS ACT 1970
The unaltered earlier Indian patent regime under 1970 Indian Patents Act
differed in many ways from that of the TRIPs agreement.
·
The Patents Act drastically restricted the
rights of patent holders in fields linked to basic needs. This is due to the
fact that the adoption of the Patents Act 1970 was based on a lengthy
legislative process and careful consideration of the socio-economic impacts of
the patents in sensitive fields such as health and food. Therefore India had to
considerably alter its patent law. In order to fully comply with the TRIPs
provisions India amended the Patents Act 1970, three times.
·
The first two amendments to the patent
legislation took place in 1999 and 2002 mainly to accommodate issues like
‘exclusive marketing rights’ (EMRs) and to extend the patent protection for the
20 years respectively. In 2005, the Patents Act 1970 has been amended for the
third time. Immediately after this amendment the scientific, technical and
business communities geared up for intense debate.
THE PATENTS (AMENDMENT) ACT, 1999
In compliance to the provision of transitional arrangement and
protection of existing subject matter as per Articles 65 and 70 of TRIPs, India
notified an amendment to the Patents Act, 1970, by proposing and introducing
·
Exclusive Marketing Rights (EMR) provisions on
1st January 1995. However, this notification failed to receive assent of the
Parliament and lapsed thereafter. Consequently, India was dragged to Dispute
Settlement Body (DSB) by United States and European Union. On receiving the
adverse judgment from DSB, India successfully enacted in the 1st Amendment
introducing the EMR provision for a period of 5 years or till the product patent
is granted or patent application is rejected, whichever is earlier and the
mailbox procedure for patent applications claiming pharmaceutical and
agro-chemical products retrospectively from 1st January 1995.[30]
·
The main objective of the Patents (Amendment) Act
1999 is to remove exclusion of product patents in the area of food, medicine
and drugs. According to the Government, this has been necessitated by India’s
obligations as a signatory to the WTO. However, by merely introducing new
clauses for exclusive marketing rights associated with product patent
applications in the area of pharmaceuticals and agrochemicals as required by
the TRIPs treaty without introducing new clauses for exclusion.
·
The Patents Act 1970 had excluded large areas
from patentability. The 1999 Act in contrast gives Exclusive Marketing Rights
(EMRs) merely on the basis of foreign patents obtained after 1 January 1995
without any scrutiny on the basis of impact on public health, public morality
or the public interest.[31]
·
The Patents (Amendment) Act, 1999 specified four
pre-conditions to be met by an EMR applicant: (a) the applicant must hold a
valid patent on pharmaceutical product granted after January 1, 1995 in any of
the WTO member countries; (b) the applicant should have marketing rights in the
member countries; (c) a product patent application should already have been
made in India, and (d) marketing approval of the same product should have been
granted in India. The first three conditions were as per the stipulation of
TRIPs agreement. The fourth clause was incorporated to meet the Indian drug
regulatory approval.
·
The other important change made was the removal
of restriction on residents to apply for patents outside India. In the Patents
Act (1970) It was obligatory for residents (section 39) to seek prior
permission before applying for patent outside India.
·
This Act sought to provide stronger patent
protection for foreign pharmaceuticals and to create stronger domestic research
capabilities. For example, an Indian company (Ranbaxy Lab, Inc.) signed a $ 90
million dollar joint venture with Eli Lilly & Co. to collaborate for
pharmaceutical research and development. These Indian patent laws could allow
the Indian pharmaceutical industry to modernize its pharmaceutical industry and
compete with the developed world.[32]
THE PATENTS (AMENDMENT) ACT, 2002
The second of the three amending Acts in the evolution of India’s patent
law towards TRIPs compliance was the Patent (Amendment) Act, 2002, effective
from 20 May 2003.The 2002 Act implemented a number of important changes, but
most significant was
·
The extension of patent term to twenty years.
Uniform term of patent protection of 20 years for all categories of invention
as per Article 33 of the TRIPs agreement has been prescribed. The 2002 Act amended
the principal Act to provide that the term of all Indian patents would
henceforth expire twenty years after their application filing date. Prior to
this amendment, Indian process patents lasted only for the shorter of 5 years
from sealing or 7 years from the date of the patent, while the term of all
other types of patents (e.g., mechanical devices) was 14 years from the date of
the patent.
·
Another notable aspect of the 2002 amendments
was formal recognition in India’s Patents Act of the nations’ accession to two
leading international intellectual property treaties, both administered by the
United Nations-affiliated World Intellectual Property Organization (WIPO). As
required by TRIPs, India brought its laws into compliance with the provisions
of the Paris Convention for the Protection of Industrial Property, which
entered into force in India on December 7, 1998. India henceforth had to abide
by the Convention’s national treatment principle, which forbids discriminatory
treatment of foreign applicants, as well as its right of priority, which allows
foreigners who have previously filed an application for patent in their home
countries a twelve-month priority period in which to file an application
directed to the same invention in India while retaining the benefit of their
earlier home country filing date.[33]
·
The Patents (Amendment) Act, 2002, implemented a
myriad of other changes intended to bring India’s patent law into accord with
the TRIPs agreement, including new definitions of ‘invention’ and ‘inventive
step’ and new exclusion from patentable subject –matter like business methods,
algorithms and traditional knowledge.
·
The amendment also reversed the burden of proof
provision involving cases of process patent, infringement and streamlined the
compulsory licensing framework.
·
The 2002 amendment also paved the way for
patentability of microorganisms.
·
The 2002 amendments are substantially different
from the 1999 draft with regard to compulsory licensing. Section 83, which
provides a general framework to guide the issuance of compulsory licences, is
particularly noteworthy. It constitutes a broader endeavour to incorporate some
of TRIPs in-built flexibility in to the Patents Act.
Interestingly, Section 83 specifically
mentions that patents granted should not “impede protection of public health”,
should not prohibit the central government from taking measures to protect
public health and the patents should be granted to make the benefits of the
patented invention available to the public at reasonably affordable prices.
·
Qualification of patent agents was amended restricting
to only science, engineering and technology graduated to be patent agents.
Additional exceptions,[34]
penalties and many other amendments were introduced to comply with TRIPs and to
balance the rights and obligations. Appellate Board for patents was introduced
under Chapter XIX, which came into effect much later in 2007.
THE PATENTS (AMENDMENT) ACT, 2005
India became a party to the TRIPs agreement in April 1994. At that time,
India’s current enactment, the Patent Act of 1970 directly contravened Article
27 of the TRIPs agreement. Upon coming into effect on January 1, 1995, TRIPs
set out transitional periods for WTO members to introduce legislation complying
with the obligations under TRIPs.
For developing countries like India, the deadline for complying with
TRIPs was the year 2000. In addition, Article 65.4 of TRIPs provided a special
transitional provision for those countries that did not grant product patents.
The provision provided an additional five years (until 2005), from the initial
TRIPs transitional period to introduce product patent protection. India took
advantage of this extra transition period. Technically speaking, only one
amendment was required under TRIPs, i.e., the introduction of product patents
for pharmaceutical inventions. However, the ordinance carried out a further 74
amendments to the Patents Act, thus taking it much beyond the TRIPs
requirements. In effect these set of amendments took India into a ‘TRIPs plus’
regime. On December 26, 2004, India issued a presidential decree to amend its
law and meet this final dead line. The Patents (Amendment) Act of 2005 passed
by the Indian Parliament, replaced that Ordinance.
Under TRIPs agreement, WTO members have to enforce product patents for
agrochemicals and pharmaceutical compounds. About 50 developing countries,
including India had not complied with this requirement during the Uruguay round
of GATT negotiations. The much awaited and debated patents amendment was
finally passed in parliament in March 2005. This third amendment to the Indian
Patents Act 1970 brought India in the line with the TRIPs agreement.[35]
Some other important changes made were:
(a) Redefining the scope of invention. Of particular significance were
(i) allowing patents for treatment of plants (medicinal, surgical, curative and
prophylactic process) to render them free of diseases or to increase their
economic value or that of their products, and (ii) allowing patents covering
microorganisms;
(b) The source of geographical origin of biological material used in
invention was made mandatory to be disclosed in the invention. A list of
Authorized Depository Institutions were notified in the gazette of India, Part
II, Section 3 for depositing the biological materials mentioned in the
specification at the time of filing a patent application.
·
India moved from a process patent system to a
product patent system in 2005. The patent law is one of the seven intellectual
property laws protected under this agreement. Section 5 of the TRIPs agreement
deals with Patents. Article 27 says that “patents shall be available for any
inventions, whether products or processes in all fields of technology provided
that they are new, involve an inventive step and are capable of industrial
application”.[36]
·
The most prominent and controversial change has
been the deletion of section 5 of the Patents Act, 1970, thereby paving the way
for product patents in the area of pharmaceutical and other chemical
inventions. Section 5 of the Patents Act, 1970 (as it stood after the 2002
amendments) had provided that, in the case of inventions being claimed relating
to food, medicine, drugs or chemical substances, only patents relating to the
methods or processes of manufacture of such substances could be obtained.
·
Act 2005 is the cornerstone provision for
bringing India’s patents law into compliance with TRIPs. Product Patent is the
granting of patent to the ‘final’ product irrespective of the process used for
obtaining the product. Once you obtain a patent on the product, then one is
precluded from manufacturing that product, even though with a different process.
·
Software Patentability Section 3(k) of the
Patents (Amendment) Act, 2005 excluded “a computer program per se” from the
scope of patentability. This exclusion met with conflicting interpretations at
the patent office, with some examiners granting patents to software combined
with hardware or software with a demonstrable technical application of some
sort. The 2004 Ordinance therefore qualified this exclusion by stating that
software with a “technical application” to industry or when “combined with
hardware” would be patentable. Owing to vigorous opposition from the free software
movement, this provision was removed from the 2005 Act. The earlier position
under the Patents Act, 1970 that a computer program per se is not patentable
now prevails.
·
Distinguishing Features of Patents (Amendment)
Act 2005 ‘New Invention’ The Patents
Amendment Act, defines the term ‘new invention’ as “any invention or technology
which has not been anticipated by publication in any document or used in the
country or elsewhere in the world before the date of filing of a patent
application with complete specification, i.e. the subject matter has not fallen
in public domain or that it does not form part of the state of the art”.43 It
appears that the intent behind this provision is to define a ‘novelty’ standard
- which, along with ‘non-obviousness’ (or ‘inventive step’) and ‘utility’
(‘industrial applicability’), are the three prerequisites for ‘patentability.
·
The
‘Inventive Step’. The 2005 Act makes a critical change to the earlier
‘non-obviousness’ or ‘inventive step’ test. The definition now reads: ‘inventive
step’ means a feature of an invention that involves technical advance as
compared to the existing knowledge or having economic significance or both and
that makes the invention not obvious to the person skilled in the art. As can
be seen from this definition, while the fundamental yardstick for measuring an
‘inventive step’ remains that which is “not obvious to a person skilled in the
art”, a requirement that the invention involve a ‘technical advance’ or have an
‘economic significance’ of some sort has been added.
·
Pharmaceutical
Substances. The introduction of a new definition for “pharmaceutical
substance” under Section 2(t a) of the Patents Act, as amended, defines a
pharmaceutical substance as “any new entity involving one or more inventive
steps”.
·
The ‘New
Use’ Exclusion. Section 3(d) of the Patents Act, 1970 excluded a “new use
for a known substance” from the ambit of ‘invention’. The 2005 Act has expanded
on this exception by providing that “the mere discovery of a new form of a
known substance which does not result in the enhancement of the known efficacy
of that substance” would not be patentable.
The new Patents Act (Patents Amendment Act
2005) has created a strong patent system in India. Overall the present Act has
increased the scope of patenting and provides stringent safeguards to the
patentee. The new Act would play a major role in creating a technology driven
market. Firms would increasingly try to create monopoly based on their patented
technology. Indian firms primarily those that are in high technology areas
would face increasing pressure, as patented products would enter the market.
WORLD INTELLECTUAL PROPERTY ORGANISATION (WIPO).
The World
Intellectual Property Organization (WIPO) is the global forum for intellectual
property services, policy, information and cooperation. WIPO is
the global forum for intellectual property services,
policy, information and cooperation. It is a self-funding agency of the United Nations, with 189
member states.
The World Intellectual Property Organization (WIPO) was
established by a convention of 14 July 1967, which entered into force in
1970. It has been a specialized agency of the United Nations since 1974, and
administers a number of international unions or treaties in the area of
intellectual property, such as the Paris and Berne Conventions.
WIPO’s
objectives are to promote intellectual property protection throughout the world
through cooperation among states and, where appropriate, in collaboration with
any other international organization. WIPO also aims to ensure administrative
cooperation among the intellectual property unions created by the Paris and
Berne Conventions and sub-treaties concluded by the members of the Paris Union.
The
administration of the unions created under the various conventions is
centralized through WIPO’s secretariat, the “International Bureau”. The International
Bureau also maintains international registration services in the field of
patents, trademarks, industrial designs and appellations of origin. WIPO also
undertakes development cooperation for developing countries through advice,
training and furnishing of documents.
An agreement on
cooperation between WIPO and the WTO came into force on 1 January
1996. The agreement provides cooperation in three main areas:
·
notification of, access to and translation of
national laws and regulations
·
implementation of procedures for the protection
of national emblems
·
And technical cooperation.[37]
The
treaties administered by WIPO fall into three groups.
A. The
first group consists of treaties which establish international protection,
that is to say, they are treaties which are the source of legal protection
agreed between countries at the international level. Four treaties on industrial property fall
into this group. They are
·
The Paris Convention for the Protection
of Industrial Property,
·
The Madrid Agreement for the Repression
of False and Deceptive Indications of
Source on Goods,
·
The Lisbon Agreement for the Protection
of Appellations of Origin and their International Registration, and
·
The Nairobi Treaty on the Protection of
the Olympic Symbol
Two
treaties in the field of copyright and neighboring rights fall into this group,
namely
·
The Berne Convention for the Protection
of Literary and Artistic Works and
·
The Rome Convention for the Protection of
Performers, Producers of Phonograms and Broadcasting Organizations
B. The
second group consists of treaties which facilitate international protection. Seven treaties on industrial property fall
into this group. They are
·
The Patent Cooperation Treaty which
provides for the filing of international applications for patents,
·
The Madrid Agreement Concerning the
International Registration of Marks,
·
The Protocol Relating to the Madrid
Agreement just mentioned (both of them provide for the filing of international
applications for marks),
·
The Lisbon Agreement which has already
been mentioned because it belongs to both the first and the second groups,
·
The Budapest Treaty on the International
Recognition of the Deposit of Microorganisms for the Purposes of Patent
Procedure,
·
The Hague Agreement Concerning the
International Deposit of Industrial Designs and
·
The Trademark Law Treaty which entered
into force on August 1, 1996.
Two
treaties in the field of neighboring rights may also be considered as falling
into this group, namely
·
The Geneva Convention for the Protection
of Producers of Phonograms Against Unauthorized Duplication of Their Phonograms
and
·
The Brussels Convention relating to the
Distribution of Programme-Carrying Signals Transmitted by Satellite.
C. The
third group consists of treaties which establish classification systems
and procedures for improving them and keeping them up to date. The following four treaties, all dealing with
industrial property, fall into this group:
·
The Strasbourg Agreement concerning
International Patent Classification (IPC),
·
The Nice Agreement Concerning the
International Classification of Goods and Services for the Purposes of the
Registration of Marks,
·
The Vienna Agreement Establishing an
International Classification of the Figurative Elements of Marks and
·
The Locarno Agreement Establishing an
International Classification for Industrial Designs.
ACTIVITIES OF WIPO
A.
Assistance to developing countries constitutes
the first pillar of WIPO’s activities, and takes the form of
1.
Training (groups and individuals, in
general or specialized courses, seminars to provide for an exchange of
information and experience),
2.
Promotion of creative activities and
of technology transfer,
3.
The provision of technological
information contained in patent documents,
4.
The provision of advice on laws and
regulations as well as
5.
The management of industrial
property offices and copyright collective administration societies, as well as
the provision of equipment.
B.
The second pillar relates to
activities in the setting of international standards and norms for the
protection and administration of intellectual property. They are concerned with
1.
Revision of existing treaties or
creation of new ones,
2.
Simplifying procedures at the
national, regional or international levels for the granting of intellectual
property rights,
3.
The effective enforcement and
protection of such rights,
4.
The efficient management of
collections of industrial property documents used for search and reference, and
devising means for making access to the information they contain easier;
5.
The maintenance and updating of
international classification systems, the compilation of statistics;
6.
Collection of laws on industrial
property and copyright law administration.
Under this heading could be included the work of the
WIPO Arbitration and Mediation Center.
Promotion of the acceptance--or wider acceptance--of treaties, by
countries is also an important activity of WIPO.
C.
The registration activities
are the third pillar of WIPO and involve direct services to applicants for, or
owners of, industrial property rights.
These activities concern the receiving and processing of international
applications for the protection of inventions, or for the international
registration of marks or deposit of industrial designs.
Thus, generally, WIPO in relation to
patent administers, protects and kind of supervises all the treaties under it
including TRIPs.
PATENT COOPERATION TREATY 1970
The
Patent Cooperation Treaty (PCT) assists applicants in seeking patent protection
internationally for their inventions, helps patent Offices with their patent
granting decisions, and facilitates public access to a wealth of technical
information relating to those inventions. By filing one international patent
application under the PCT, applicants can simultaneously seek protection for an
invention in a very large number of countries.
Signed
in June 1970, in Washington, D.C., and became operational in June 1978 with 18
States.
The
PCT is an international treaty with more than 145 Contracting States. The
PCT makes it possible to seek patent protection for an invention simultaneously
in a large number of countries by filing a single “international” patent
application instead of filing several separate national or regional patent
applications. The granting of patents remains under the control of the national
or regional patent Offices in what is called the “national phase”.
THE PCT PROCEDURE INCLUDES:
Filing: you file an international application with a national or
regional patent Office or WIPO, complying with the PCT formality requirements,
in one language, and you pay one set of fees.
International Search: an “International Searching Authority” (ISA) (one of
the world’s major patent Offices) identifies the published patent documents and
technical literature (“prior art”) which may have an influence on whether your
invention is patentable, and establishes a written opinion on your invention’s
potential patentability.
International Publication: as soon as possible after the
expiration of 18 months from the earliest filing date, the content of your
international application is disclosed to the world.
Supplementary International Search (optional): a second ISA identifies, at your
request, published documents which may not have been found by the first ISA
which carried out the main search because of the diversity of prior art in
different languages and different technical fields.
International Preliminary Examination (optional): one of the ISAs at your request,
carries out an additional patentability analysis, usually on an amended version
of your application.
National Phase: after the end of the PCT procedure, usually at 30 months
from the earliest filing date of your initial application, from which you claim
priority, you start to pursue the grant of your patents directly before the
national (or regional) patent Offices of the countries in which you want to
obtain them.[38]
ADVANTAGES OF PCT
1.
applicants have up to 18 months more than if
they had not used the PCT to reflect on the desirability of seeking protection
in foreign countries, appoint local patent agents in each foreign country,
prepare the necessary translations and pay national fees;
2.
Applicants
can rest assured that, if their international application is in the form
prescribed by the PCT, it cannot be rejected on formal grounds by any
designated office during the national phase;
3.
On
the basis of the international search report and the written opinion,
applicants can evaluate with reasonable probability the chances of their
invention being patented;
4.
Applicants
have the possibility, during the optional international preliminary
examination, to amend the international application and thus put it in order
before processing by the various patent offices;
5.
The
search and examination work of patent offices can be considerably reduced or
eliminated thanks to the international search report, the written opinion and,
where applicable, the international preliminary report on patentability which
are communicated to designated offices together with the international
application;
6.
Since
each international application is published with an international search
report, third parties are in a better position to formulate a well-founded
opinion about the potential patentability of the claimed invention; and
7.
For
applicants, international publication puts the world on notice of their
applications, which can be an effective means of advertising and looking for potential
licensees.
Ultimately,
a. Brings the world within reach
b. Postpones the major costs associated
with internationalizing a patent application
c. Provides a strong basis for patenting
decisions
d. Used by the world’s major corporations,
universities and research institutions when they seek international patent protection
e. Allows you to apply securely and
easily online, and to save money by doing so.[39]
The
PCT created a Union which has an Assembly. Every State party to the PCT is a
member of the Assembly. Among the most important tasks of the Assembly are the
amendment of the Regulations issued under the Treaty, the adoption of the
biennial program and budget of the Union and the fixing of certain fees
connected with the use of the PCT system.
PATENT LAW TREATY 2000
The
Patent Law Treaty (PLT) was adopted in 2000 with the aim of harmonizing
and streamlining formal procedures with respect to national and regional patent applications
and patents and making such procedures more user friendly. With the significant
exception of filing date requirements, the PLT provides the maximum sets of
requirements the office of a Contracting Party may apply. The PLT was concluded
in 2000, and entered into force in 2005.
The
PLT is open to States members of WIPO and/or States party to the Paris
Convention for the Protection of Industrial Property (1883). It is also open to
certain intergovernmental organizations. Instruments of ratification or
accession must be deposited with the Director General of WIPO.[40]
OBJECTIVES OF PLT
1.
Unification
of patent law
2.
Simplify
procedure
3.
Reduce
cost
4.
Enable
that offices maintain quality
5.
Avoid
duplication
6.
Meet
needs of large and medium offices
7.
Assist
developing countries
GENERAL RULES OF PATENT LAW TREATY
A.
Offices must award a filing date to applicants with 3 requirements.
B.
Content of international applications must be documented.
C.
A specified model for international forms.
D.
Priority should be give based of first to file.
E.
Sufficient disclosure.
F.
Novelty.
G.
Grace period
The
PLT is open to States members of WIPO and/or States party to the Paris
Convention for the Protection of Industrial Property (1883). It is also open to
certain intergovernmental organizations. Instruments of ratification or
accession must be deposited with the Director
CONCLUSION
All
of these conventions have one way or another contributed positively and
negatively to the subject matter of Intellectual property and patent as a case
study. However, I would not fail to say that each of them has their loopholes
from which the laws get bent and most times broken.
With
all these international laws, where is the scope for proper sovereign laws by a
state for its own citizen? Seeing that even the liberty given to make law is
still limited to certain provisions.
Any
loopholes in the laws in relation to intellectual property would be the
downfall of not just a state’s economy but the world at large.
BIBLIOGRAPHY
TEXTBOOKS
a.
Dr. Elizabethan Verkey, Law of Patents, (2nd ed.
2012)
b.
P. Narayanan, Intellectual Property Law, (3rd ed. 2001)
c.
Dr. S.K Singh, Intellectual Property Rights Laws, (2nd ed. 2013)
d.
Dr. S.R Myneni, Law of intellectual property, (7th ed. 2015))
JOURNALS,
MAGAZINES, BLOGS AND WEBSITES
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Protection of
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available at http://www.altacit.com/publication/protection-of-intellectual-property-rights-under-the-indian-and-international-laws/#i_2, last seen on
25/02/2017.
b.
[1] Benita Ezeigbo, Major
international conventions protecting intellectual property, Miss Benny,
available at http://bennylegal.blogspot.in/search?updated-max=2017-02-23T09:24:00-08:00&max-results=7, last seen on
25/02/2017.
c.
World
Intellectual Property Organsation, Paris
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25/02/2017.
d.
Seth
M. Reiss Lex-IP.com Honolulu, Hawaii, Commentary
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e.
World
Trade Organisation, The GATT years, from
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26/02/2017.
f.
Manjunath abv. Influence of GATT on the Indian economy, author stream, available
at
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last seen on 26/02/2017.
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World
Trade Organisation, Understanding the WTO
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26/02/2017.
h.
Koel Roy, The
Internalisation Of Patent Laws.
i.
Fredrick M.
Abbot, “First Report to the Committee on International Trade Law of the
International Law Association on the Subject of Parallel Importation”, Journal
of International Economic Law, 1998, p. 607
j.
P.
Danzobn, “Differential Pricing for
Pharmaceuticals: Reconciling Access, R&D, and Intellectual Property”,
CMH working paper series paper No WG2:10, 2001.
k.
Gopakumar
G. Nair, “Impact of TRIPs on Indian Pharmaceutical Industry”,
Journal of Intellectual Property Rights, Vol. 13, September 2008, p.436.
l.
Vandanashiva,
Patents Myths and Reality, (New
Delhi: Penguin Books India (P) Ltd., 2001), p.104.
m.
Angela
J. Anderson, “Global Pharmaceutical
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Shodhganga,
Influence of TRIPs on Indian Patent Law,
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World
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World
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The International Patent System, available at http://www.wipo.int/pct/en/,
last seen on 02/03/2017.
ACTS
a.
Indian Patent Act of 2005.
b.
Indian Patent Act of 1970.
[1] Dr. S.K. Singh, Intellectual Property Right Laws, 91, (2nd
ed.2013)
[2]Protection
of intellectual property rights under the Indian and international law, Altacit Global, available at http://www.altacit.com/publication/protection-of-intellectual-property-rights-under-the-indian-and-international-laws/#i_2, last seen on 25/02/2017.
[3]
Benita Ezeigbo, Major international conventions protecting
intellectual property, Miss Benny, available at http://bennylegal.blogspot.in/search?updated-max=2017-02-23T09:24:00-08:00&max-results=7, last seen on 25/02/2017.
[4]
World
Intellectual Property Organsation, Paris
convention for the protection of Industrial property, available at http://www.wipo.int/treaties/en/text.jsp?file_id=288514, last seen on 25/02/2017.
[5] Seth M. Reiss Lex-IP.com
Honolulu, Hawaii, Commentary on the Paris
convention for the protection of industrial property, available at http://www.lex-ip.com/Paris.pdf, last seen on 25/02/2017.
[6] Ibid.
[7] Ibid.
[8] Ibid.
[9] Supra note 5.
[10]
World
Trade Organisation, The
GATT years, from Harvana to Marrakesh, available at https://www.wto.org/english/thewto_e/whatis_e/tif_e/fact4_e.htm, last seen on 26/02/2017.
[11]
Manjunath abv. Influence of GATT on the Indian economy, author
stream, available at http://www.authorstream.com/Presentation/manjunathabv-1355567-influence-of-gatt-on-the-indian-economy/, last seen on 26/02/2017.
[12]
World
Trade Organisation, Understanding the WTO agreements, available at https://www.wto.org/english/thewto_e/whatis_e/tif_e/agrm7_e.htm,
last seen on 26/02/2017.
[13] Koel Roy, The Internalisation Of Patent Laws.
[14] Fredrick M. Abbot, “First Report to the Committee on
International Trade Law of the International Law
Association on the
Subject of Parallel Importation”,
Journal of International Economic Law, 1998, p. 607.
[15]
P. Danzobn, “Differential Pricing for Pharmaceuticals:
Reconciling Access, R&D, and Intellectual Property”, CMH working paper
series paper No WG2:10, 2001.
[16] Ibid.
[17] Article 27(3)of TRIPs Agreement.
[18]
Article 27 (2) of TRIPs
Agreement
[19]
Article 27 (3) b of TRIPs
Agreement
[20] Article 28 of TRIPs Agreement
[21] Article 28.2 of TRIPs Agreement
[22]
Compulsory licensing for a
whole class of products such as all medicines would not be acceptable.
[23]
Supra note 13.
[24]
Article 28.2 of TRIPs
Agreement
[25]
Article 65 (4) b of TRIPs
Agreement
[26]
Article 70.8 of TRIPs
Agreement.
[27]Article 70.9 of TRIPs Agreement
[28] Supra note 12.
[29]It provides that the protection
and enforcement of intellectual property rights should contribute to the
promotion of technological innovation and to the
transfer and dissemination of technology, to the mutual
advents of producers and users of technological
knowledge and in a manner conducive to social and
economic welfare, and to a balance of rights and
obligations
[30] Gopakumar G. Nair, “Impact of TRIPs on Indian Pharmaceutical Industry”,
Journal of Intellectual Property Rights, Vol. 13, September 2008, p.436.
[31] Vandanashiva, Patents Myths and Reality, (New Delhi:
Penguin Books India (P) Ltd., 2001), p.104.
[32]
Angela J. Anderson, “Global Pharmaceutical Patent Law in
Developing Countries – Amending TRIPS to Promote Access for All”, bepress
Legal seris, 2006, http://infojustice.org/download/pdf. Accessed on 10-5- 2010.
[33]
Dr. Rajeshkumar Achary, “Recent Changes in Patent Laws: India”, available
at http:/ /www .sristi. org/mdpipr 2004 /day1/D1S1R1.doc. last seen on
01/03/2017.
[34] Section 107A, Patents Act, 1970.
[35]
Shodhganga, Influence of TRIPs on Indian Patent Law, available
at http://shodhganga.inflibnet.ac.in/bitstream/10603/21666/9/chapter-vi.pdf, last seen on 01/03/2017
[36] Ibid
[37]World Trade Organisation, What is WIPO? available at https://www.wto.org/english/tratop_e/trips_e/tripfq_e.htm#WIPO, last seen on 02/03/2017.
[38]
World Intellectual Property
Organisation, PCT- The International
Patent System, available at http://www.wipo.int/pct/en/, last seen on 02/03/2017
[39] Ibid
[40] Supra note 38.
Thanks for the information.
ReplyDeleteNadia
Probate Attorney in San Bernardino