NEW YORK (GenomeWeb News) – The US House of Representatives this week passed the Food and Drug Administration Reform Act, which would reauthorize the Medical Device User Fee Act and implement a number of medical device regulatory reforms, with strong bipartisan support.

The House passed the bill on a vote of 387 to 5, and followed swiftly after the Senate passed its own version of the act last week with overwhelming support.

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In Science this week: caution urged in use of gene drives, and more.

NIH's Sally Rockey examines the tapped and untapped potential of the NIH peer reviewer pool.

PLOS Biology has asked researchers how they envision the future of genetics and genomics.

Representative Lamar Smith brings back a provision to require the National Science Foundation to certify that each study it funds is "in the national interest."