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: factors influencing retrotransposon integration sites, and more.

A bioethicist argues for the responsible use of germline gene editing.

Some breweries are using DNA-based testing to determine whether unwanted bacteria are affecting their beers, The Verge reports.

Standardized N-of-1 trials will be needed to test out personalized medicines, writes Nicholas Schork from the J. Craig Venter Institute at Nature.