Association of Clinical Research Organizations Calls for Additional Funding for FDA’s Overseas Offices

WASHINGTON--(BUSINESS WIRE)-- The Association of Clinical Research Organizations, which represents the global CRO industry, issued the following statement in response to the Government Accountability Office’s report on the Food and Drug Administration’s Overseas Offices.

“The members of ACRO conduct ethical, high-quality clinical research in more than 115 countries,” said Doug Peddicord, Ph.D., Executive Director. “A strong global regulatory regime is imperative to maintain confidence in this important research and the world looks to the U.S. FDA as the leading regulatory authority. For these reasons, ACRO this year has been advocating for increased appropriations for the FDA’s Office of International Programs. Congress must provide the OIP with additional resources so it may carry out its critical role in overseeing foreign clinical trials, as well as its responsibilities to ensure the safety of imported drugs and food.”

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About ACRO

The Association of Clinical Research Organizations (ACRO) represents companies whose focus is clinical research. The association provides an active voice for the global CRO industry, which provides specialized services that are integral to the development of drugs, biologics and medical devices. Through its member companies, ACRO helps improve the quality, efficiency and safety of biomedical research. ACRO member companies employ approximately 70,000 professionals worldwide and annually conduct more than 9,000 clinical trials involving nearly two million participants in 115 countries. For more information, please visit


Association of Clinical Research Organizations (ACRO)
John Lewis, 202-464-2310
[email protected]

KEYWORDS:   United States  North America  District of Columbia

INDUSTRY KEYWORDS:   Stem Cells  Health  Biotechnology  Clinical Trials  Public Policy/Government  Healthcare Reform  Pharmaceutical  Public Policy  White House/Federal Government  FDA