In the process of wooing foreign investment through alignment of
Indian IP laws with global standards, we must not dismiss the concerns of or
sacrifice the interests of the Indian industry. On April 24, 2015, it was reported
that the Prime Minister Shri Narendra Modi has called for aligning India’s
patent law with “global standards” to boost trade. There’s also talk of putting
in place “IPR Guidelines” which match “global standards”. Before India proceeds
to amend its patent law to “align it with global standards” or issues “IPR
Guidelines” with the object of boosting trade, a few fundamental questions need
to be asked.
What is so wrong about our patent law which calls for an
amendment? Is the legislation, the Patents Act, 1970, flawed or deficient in
protecting the rights of an innovator/patentee? Or is the quality of enforcement
of IP in India by our Courts the issue? Importantly, whose IP are we talking
about protecting here? What are these “global standards”,if there is one? Will
the proposed “IPR Guidelines” have the force of law? Who is expected to adhere
to these guidelines? In addressing these questions, clarity on certain cardinal
aspects of the patent regime is necessary. It must be understood that the
current Indian patent regime is a mix of mandatory obligations cast on India as
a signatory to TRIPs, and certain policy decisions taken by India in exercise
of flexibilities provided under TRIPS (Agreement on Trade-Related Aspects of
Intellectual Property Rights) to member nations to address their national
interests. This means although there are certain minimum mandatory universal
requirements India’s patent law must conform to, the grant of the right and its
enjoyment are based on India’s standards of patentability and Indian
limitations on patent rights.
Importantly, the territorial scope of a patent
right is limited to the country of its grant. These factors lend to patents
their territorial nature. Simply put, there is no concept of a universal patent
(although there are regional patents such as the ones granted in the EU).What
must also be noted is that TRIPS forbids any signatory from discriminating
against owners of IP based on nationality. This is known as the principle of
“national treatment” of right owners. Should any signatory violate any of its
obligations under TRIPS, the country alleging violation may initiate
proceedings against India before the WTO Dispute Resolution panel. The question
that now arises is, in light of the national character of a patent right, what
has occasioned this talk of aligning India with “global standards” when in the
negotiations on TRIPS, the objective of India and other similarly placed
countries was to preserve their sovereign right to protect their respective
national interests? It is safe to assume that this gradual chorus for “global
standards” is attributable to the following: a. The contention of right owners in
the pharmaceutical space that Section 3(d) of the Patents Act (which
effectively prevents ever-greening of patents over drugs, among other things)
is not TRIPS-compliant. Readers may recall this provision was successfully
applied by the Indian Supreme Court to reject Novartis’s Indian Patent
application on its anti-cancer drug Gliveca. The apprehension of frequent use
of the compulsory licensing mechanism under the pretext of securing public
interest.
For instance, the issuance of a compulsory license in favour of NATCO
for Bayer’s patented drug Nexavar (which is used to renal carcinoma) resulted
in a massive reduction of the price of the drug. a. Perceived lack of
enforcement of patents of non-Indian
right owners by Indian Courts It is worth noting that Novartis’s writ petition
challenging the constitutionality of Section 3(d) for alleged violation of
TRIPS was rejected by the Madras High Court in 2007, and the decision was never
appealed against by the company. Also, as the author has argued in this article
on the 2012 Novartis decision of the Supreme Court that if any country, which is
party to TRIPS, were to challenge the legitimacy of Section 3(d) before the WTO
Dispute Resolution Panel, India is not without legally sound arguments to
support its existence. In fact, support for Section 3(d) may be drawn from
Article 27 of TRIPS which it allegedly violates. Therefore, Section 3(d) is no
reason to amend the Patents Act nor should its rigour be whittled down given
that it serves to protect public interest .As for the apprehended frequent use
of the compulsory licensing mechanism, to quote an adage one has often heard,
one swallow doesn’t make a summer. Unless there is a politically motivated
pattern that anyone is capable of objectively demonstrating in India’s use of
the compulsory licensing mechanism, the mechanism per se is not violative of
TRIPS since Article 31 of TRIPS, in spirit, permits it.
In fact, the Doha
Declaration on the TRIPS agreement and Public health expressly recognizes the
right of member countries to grant compulsory licenses to protect public
health. If the issue is about the use of the mechanism thus far by India, in
the facts of the Bayer case, it would take some mind-boggling jugglery of facts
to argue that it wasn’t a fit case for grant of a compulsory license in light
of Bayer’s anti-cancer drug’s (Nexavar) scant availability in India and its
exorbitant pricing (under the Patents Act, reasonable affordability and
availability of a patented product are mandatory requirements a patentee is
expected to fulfil). Pertinently, grant of compulsory licenses is not peculiar
to India. Mature patent jurisdictions like Canada and Belgium too have compulsory
licensing regimes which have been used in the past. Clearly, it is premature to
accuse the Indian mechanism of abuse given that instances of its use haven’t
yet attained a critical mass. On the issue of enforcement of patents of
non-Indian right owners by Indian Courts, what must be clearly understood is
that by and large the decision of a Court is a contextual enquiry based on
application of law to a given factual matrix. Therefore, one must be careful in
generalizing these decisions. Also, merely because Indian Courts have advocated
caution in enforcing pharma-related patents, it does not render the approach
counter to TRIPS, nor has the application of this cautious approach been
exclusively restricted to non-Indian IP owners. It is a principle culled out
from common law to protect public interest.
Factually too, it is untrue that
pharma-related patents haven’t been enforced by Indian Courts ever. As recently
as March 2015, the Delhi High Court granted a temporary injunction against an
Indian generic company in favour of Merck, a global major, with respect to
Merck’s patented anti-diabetes drug Sitagliptin. Although this matter is
currently pending before the Supreme Court, the point to be noted is that it
would be untrue and unfair to allege discrimination against non-Indian IP
owners. On the contrary, over the last two years, our Courts have, at regular
intervals, grant edex part e orders in favour
of global giants, particularly in the telecom space, which are perhaps not in
consonance with “global standards”. Therefore, this perception that Indian Courts
are inherently averse to enforcing IP owned by non-Indian entities has no
factual basis. One would in fact go a step further to say that our current
patent enforcement regime goes well beyond the minimum obligations under TRIPS.
India has provided for border control measures in the form of IPR Enforcement
Rules, 2007 which permits IP owners, including a patent owner to seek seizure
of allegedly infringing goods based on assessment of the allegation by the
Customs Commissioner. This is clearly over and above the minimum mandate of
TRIPS because a Customs Commissioner has been vested with the power to decide
as complex an issue as patent infringement which even Courts are expected to
approach with great caution. The Delhi High Court has even acknowledged this problem
in a decision. Fortunately, the application of the IPR Enforcement Rules to
patent matters has been challenged in a writ petition before the Delhi High
Court and hopefully, the position is expected to be clear by the end of this
year. As regards formulation of “IPR guidelines” by the Centre, when there
exist IP legislations whose interpretation and enforcement is the exclusive
prerogative of Courts and quasi-judicial authorities, it is best to avoid
formulating guidelines which deal with IPR enforcement if the doctrine of
separation of powers is to be respected. Instead, it would help to look into
other factors which also contribute to creating a culture of innovation in a
country which is not exactly resource-rich.
The government would do well to
draw lessons from countries such as Germany and Israel whose achievements in
the sphere of innovation are truly monumental. After all, it makes better sense
to not put all our eggs in the IP enforcement basket alone. In light of these
facts, one honestly wonders as to what is the basis for seeking to align our
patent law with “global standards”. If global standards are what we wish to
align with, we should know that increasingly, mature IP jurisdictions are
moving towards a more cautious and nuanced approach to the enforcement of
patents given the anti-market and anti-trust implications of indiscriminate
enforcement. One does not wish to take the position that patents are per se bad
or that they epitomise capitalistic greed, because in the real world, where
recovery of investment is indeed a motivating factor that drives R&D, until
a better and realistic alternative to IP rights is created, IPR plays a central
role and so does its enforcement.
However, the short point is, to reduce the
issue of investment to a patent-centric debate does not do justice to the
subject, and in fact does disservice to the broader discourse on furthering
innovation and incentivising investment. Critically, the implications of brash enforcement
of IP on competition in the market is an area where scholarship is one the rise
and those interested in “aligning our patent law with global standards” would
do well to pay attention to it.In the process of wooing foreign investment
through alignment of Indian IP laws with global standards, we must not dismiss
the concerns of or sacrifice the interests of the Indian industry. After all,
“Make in India” would be truly a success only when Indians play the most
significant role in turning India into a manufacturing hub. Finally, a BJP-led
Government must not contribute to the weakening of “swadeshi” interests and
certainly cannot be seen as doing so. Surely, this Government is capable of a
more nuanced approach to boosting trade and investment in India.
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