E-drug: Bad cop, more bad cops, Geneva negotiations on para 6
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Notes on Geneva negotiations on paragraph 6
(how the WTO plans to get its bad reputation back)
USA
As one might expect from past history, the USA is playing the role of bad
cop on many issues in the current Doha para 6 negotiations, particularly on
the issue of the scope of diseases and the countries that can benefit. The
US wants to limit the scope of the "solution" to only a few words taken out
of context in a single paragraph on the Doha Declaration, which actually
changes the meaning of the Declaration text. One only needs to read the
various PhRMA letters and the letter from Rosa Whitaker to see what is going
on here. For the US, its favorite Doha text is last part of paragraph 1,
which says: "especially those resulting from HIV/AIDS, tuberculosis, malaria
and other epidemics." Least favorite Doha text is from paragraph 4, which
reads:
"the Agreement can and should be interpreted and
implemented in a manner supportive of WTO Members'
right to protect public health and, in particular,
to promote access to medicines for all."
Major US goal in negotiations is to make paragraph 4 more or less disappear.
The US is also leading the divide and conquer effort, with massive
pressure (particularly back home) on developing countries to fall in line,
and this is having a huge effect on African, and several Asian and Latin
American countries. Some developing countries also seem to have been
persuaded by the US story that the more it is impossible to import from
India, China or Brazil, the better for their own domestic industry, which of
course shows zero appreciation for how one would actually build up a
domestic industry. In the USA, the big PhRMA fire power is coming from the
White House, and US negotiators have almost no real freedom at this point.
EC/DG-Trade
Pascal Lamy and Paul Vandoren have pushed for a set of highly regulatory and
restrictive "safeguards" on exports, which include for example,
requirements on the packaging of generic products, notification to
patent owners and the WTO, and a series of obligations to control
diversion. Among other things, a government that authorizes exports
must notify the TRIPS council itself for each authorization,
including the terms of each license. This is an astonishing
expansion of the WTO role in micromanaging the patent license,
reaching down to every individual license, and creates an expectation
that patent owners themselves will have discussions with the TRIPS
council if the various conditions, limitations and burdens are not
sufficiently addressed.
Note here that there is zero evidence that *generic* products have been
diverted in any significant way to the EU market. (Problems have been for
branded products under patent). DG-Trade is facing a domestic rebellion,
as the French President, the Belgium Parliament and the EU parliment have
endorsed the NGO position on the use of a simple Article 30 approach.
Remarkably, developing countries have not made any points on Lamy's lack of
domestic support for the DG-Trade efforts to protect GSK and other EU firms,
nor has there been any discussion of the language of the EU Parliament
Amendment 196, which is a radically different approach. The EU also gets
some special bad cop credit for not explaining that it plans to solve its
own 31.f problem by creating a "community patent" that will legalize cross
border compulsory licensing in Europe, a "solution" that will be highly
restricted for developing countries in the Nov 24 text.
Japan.
Japan gets a prize for demanding that vaccines be excluded from the
solution, on the grounds that vaccines technically aren't pharmaceutical
products. Vaccines were eliminated from the November 24 draft of the
"solution."
Canada and Australia
Canada and Australia get honorable mention for helping the big guys beat up
on the little guys. Canada gets special bad cop credit for somehow keeping
its own Article 30 export provisions secret from most negotiators, and at
one point actually denying that such a proceeding or provision existed. In
the Canada case, Canada won the right to non-voluntary export of products
for foreign registrations of generic products, without notice to patent
owners, and without any safeguards in foreign markets, on the grounds that
patent owners can hire lawyers in export markets to protect their interests,
and with the understanding the medicines are regulated and patent owners
will generally know when an infringing product shows up in the market. But
I guess this "solution" is only available for the US, Canada and the EU
(under proposed changes in the EU medicines directive).
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James Love, Consumer Project on Technology
http://www.cptech.org,
voice: 1.202.387.8030; mobile 1.202.361.3040
James Love <james.love@cptech.org>
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