AST week, Congress, after what seemed
like an eternity of agonizing debate, finally passed the first piece of
legislation since the 1988 Generics Law aimed at rationalizing the
pharmaceutical industry in this country. The approval came almost four years
since a bill to amend the Intellectual Property Code of the Philippines to
unburden the Intellectual Property Office of decades of pro-foreign business
rulings and precedents that tied up local companies in knots whenever they
attempted to take advantage of lapsing patents to produce cheaper medicines for
Filipinos.
With the new legislation, it will no longer be possible for
pharmaceutical giants (particularly those who are American-based) to prolong for
long periods of time their monopolies on drugs that they had long before
introduced into the Philippine market. Interestingly, the long debates
highlighted the great differences in style, mind-set, and attitudes of the two
chambers of Congress.
To begin with, there was considerable wrangling between the
two chambers regarding what to call the bill. The final agreed short name of the
Bill is "Universally Accessible Cheaper and Quality Medicines Act of 2008". On
this score, it appears that the more populist-leaning House won over the upper
crust pretensions of the Senate that preferred the word "affordable" over
"cheaper".
There were other more critical differences that delayed quick
agreement in the bicameral conference committee. A thorough reading of the final
bill reveals some serious omissions and changes in language that could
critically hamper the intended effects of the bill.
The obviously pro-business Senate panel blocked all House
attempts to include any provisions that would allow the possibility of a strong
price regulatory regime. Even the compromise agreement that gave authority to
the Executive Branch to impose price controls based on certain conditions were
significantly diluted by allowing price controls only in case of "health
emergency." In very early discussions, it had been suggested that mere
certification of a "public health need" would have been sufficient to trigger a
price regulation process as well as compulsory licensing by patent-holders. This
is in fact the wording of the Doha Declaration that allows countries to lift
intellectual property restrictions on the production of medicines that are
important to their public health programs.
The other deletion that effectively diluted the effects of
the bill was the dropping of the "generics only" provision of the sections
amending the Generics Law of 1988. This provision would have prohibited
physicians to write brand names of drugs on prescriptions and would have
required drug companies to completely revise their marketing practices. Again,
in this instance, the House contingent, whose members included some very
ardently pro-poor congresspersons including physicians, had to buckle under to
their insistently pro-business Senate colleagues.
What was even more curious was the role played by the
Executive Branch in the discussions of the bill. The "generics only" provision
was actually included upon the suggestion of the Department of Health in the
Technical Working Group of the House Committee deliberations. When the medical
profession and the pharmaceutical industry loudly protested, Malacañang stepped
in to order the DOH to withdraw support for the provision. Eventually, when some
administration congressmen persisted in supporting "generics only" prescribing,
the Palace used its clout with the House leadership to quell a budding
mini-revolt. Thus it was that another "pro-poor" feature of the legislation
finally bit the dust.
In summary, what the advocates for reform in the
pharmaceutical industry got was a little bit less than half a loaf of
legislation to put pressure on prices of medicines to come down. The provisions
revising parts of the Intellectual Property Code will help local firms with
established capacities to provide better competition to the multinationals.
However, the mechanisms necessary to ensure that this enhanced competitiveness
translates into a better deal for the Filipino have been weakened to near
impotency.
When the Lower House debated its version in the 13th
Congress, there were loud accusations of a multi-million peso lobby fund against
its enactment. To be sure, there is absolutely no evidence that any blatant
lobbying, least of all by multinational companies, ever took place, at least in
this 14th Congress. Nevertheless, there is no question that this watered down
bill is much more favorable to the business sector (both local and foreign) than
had been anticipated. Since most members of the delegation from the Lower House
appeared to be fully supportive of strong anti-business measures, the question
now is who was lobbied by whom?
Unfortunately, the enthusiastic media coverage of the arguments in Congress
simply served to heighten expectations of people that prices of medicines will
drop dramatically soon. Because Congress has passed to the Executive Branch the
responsibility for ensuring that this happens, the ball is now in Malacañang’s
court. Considering this administration’s tendency to indecision on issues,
especially when business is affected, people should not be too disappointed if
the "cheaper medicines law" turns out to be a dud.