By Terri Moon Cronk DoD News, Defense Media Activity
WASHINGTON, Jan. 16, 2018 — The Defense Department and Food
and Drug Administration launched a joint pilot program to prioritize
efficiently developing safe and effective medical products to save the lives of
U.S. warfighters, officials of the agencies announced this morning in a media
teleconference.
“The partnership we announced today reflects the invaluable
collaboration between our organizations,” Tom McCaffery, acting assistant
secretary of defense for health affairs said.
“It strengthens our ability to equip our troops with the
best possible medical support, and it helps us achieve our mission of providing
battlefield care to support our entire military’s effort to achieve a safer,
more secure world,” he added.
The FDA is fully committed to working closely with DoD to
expedite availability of medical products that are critical to the health of
service members, particularly those used to treat injuries in battlefield
settings, said FDA Commissioner Dr. Scott Gottlieb, a physician and medical
policy expert.
“Ensuring our nation’s warfighters have safe and effective
medical products is a top priority for the agency,” he said. “By standing up a
collaborative program with DoD, we hope to address DoD’s immediate product
priorities and ensure these products are developed and made available in the
most expeditious manner possible.”
Quick Access Is Critical
Fast access to lifesaving medical products on the
battlefield is part and parcel of DoD’s efforts to support forces operating
around the world, McCaffery said.
“[It’s also] essential to upholding our responsibility to
the men and women of our military who risk their lives for us,” he added.
FDA’s expertise and guidance will help DoD put the best,
most-effective products in the hands of battlefield medical personnel, he
emphasized. “We look forward to working with our FDA partners on this important
pilot program to ensure delivery of critical battlefield medicine to our
deployed troops around the world.”
The framework for the program was put in place through House
Res. 4374, which authorized DoD to request, and the FDA to provide, assistance
to expedite development, in addition to the FDA’s review of products to
diagnose, treat or prevent serious or life-threatening diseases or conditions
facing American military personnel, according to an FDA press release.
Working Closely on Needs
Using the law’s expanded authorities, FDA will work closely with
DoD’s Health Affairs to better understand the military’s medical needs for
deployed personnel, give the highest level of attention to and expedite its
review of priority DoD medical products, provide ongoing technical advice to
Health Affairs to rapidly develop and manufacture medical products for use by
the military, and take a closer look at products under development for
opportunities to push their availability, the release said.
While the availability of biological items such as blood
products takes priority, the FDA and DoD are aware of the need for a broad
range of medical products for service members -- such as preventive vaccines
and therapeutics -- and these needs will continue to evolve in the future, the
FDA release said.
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