The FDA has unveiled a new program
designed to boost the number and variety of
generic-drug products over the next few years. The plan, known as
the Generic Initiative for Value and Efficiency, or GIVE, involves significant
staffing increases for the FDA generic-drug review team, as
well as a streamlined approval system that officials predict will
bring important generic products to the market "much faster" than
the current approach.
"Generic drugs generally cost less than their brand-name counterparts,
and competition among generics has been a key factor in
lowering drug prices," the FDA said in announcing the new initiative.
"The GIVE plan outlines ways to maximize the use of our
resources so that [the] FDA can review and approve even more
high quality generic drugs during the upcoming fiscal year than it
did in 2007."
The agency's efforts to bring cost-saving generic drugs to pharmacy
shelves is already paying off, with generic-product approvals
climbing 30% in fiscal year 2007 to a record 682 drugs. To boost
that approval rate even faster, the GIVE initiative empowers the
FDA to revise the review order for certain drug applications to
place extra emphasis on generics expected to have substantial
market impact.
As an example, FDA Generic Drug Director Gary Buehler explained
that "first generic products," for which there are no blocking patents
or exclusivity protections on the reference listed drug, will be earmarked
by the agency for expedited review."This will mean that these
products, for which there are currently no generic products on the
market, may reach the consumer much faster," agency officials said.
The GIVE initiative also calls for hiring and training new staffers to
bolster the 215 FDA employees currently assigned to reviewing
generic-drug applications.The FDA also plans to place more emphasis
on the use of electronic programs for handling drug submissions
and internal documents. Additionally, the FDA said that the agency
will increase its communications with generic-drug manufacturers
to help sponsors of these products submit clean applications that
can be processed with minimal delay. For a related article, please
visit www.pharmacytimes.com/give.