-- Robert Preidt
MONDAY, June 20 (HealthDay News) -- The U.S. Food and Drug
Administration announced Monday a new strategy to help ensure the
safety and quality of imported drugs and food products.
The plan, which calls for coalitions of international regulators
and increased data sharing, was created in response to rapidly
rising imports of FDA-regulated products and a complex global
supply chain. The strategy is outlined in a special report called
Pathway to Global Product Safety and Quality, the agency said in a news release.
"Global production of FDA-regulated goods has exploded over the past 10 years. In addition to an increase in imported finished products, manufacturers increasingly use imported materials and ingredients in their U.S. production facilities, making the distinction between domestic and imported products obsolete," FDA Commissioner Dr. Margaret A. Hamburg said in the news release. "There has been a perfect storm -- more products, more manufacturers, more countries and more access. A dramatic change in strategy must be implemented."
To protect the health of U.S. consumers, the FDA needs to modify
the way it conducts business and to act globally, according to the
report. This new approach includes four main elements:
The FDA said it's also expanding its food-safety efforts under
the FDA Food Safety Modernization Act (FSMA). There will be new
inspection mandates, including one to inspect more than 19,000
foreign-food facilities by the year 2016.
"FDA-regulated imports have quadrupled since 2000," Hamburg said. "The FDA and our global regulatory partners recognize this new reality and realize we must work proactively and collaboratively to address the challenges we face."
The FDA offers consumer information about a
number of products.
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