United States:
FDA Publishes Modifications To Consensus Standards For Medical Devices
27 October 2014
Jones Day
To print this article, all you need is to be registered or login on Mondaq.com.
In the October 17, 2014, Federal Register, FDA announced certain
additions, withdrawals, corrections, and revisions of consensus
standards the Agency will recognize for use in premarket
submissions and other requirements for devices. These modifications
will be incorporated in the list of FDA Recognized Consensus
Standards in the Agency's searchable database.
The content of this article is intended to provide a general
guide to the subject matter. Specialist advice should be sought
about your specific circumstances.
POPULAR ARTICLES ON: Food, Drugs, Healthcare, Life Sciences from United States
FDA Ramps Up Actions On PFAS
Holland & Knight
The U.S. Food and Drug Administration (FDA) has increased regulatory activity with regard to per- and polyfluoroalkyl substances (PFAS).
Planning For The BIOSECURE Act
Foley Hoag LLP
Bipartisan legislation moving through the U.S. House and Senate, known as the BIOSECURE Act, could limit the ability of U.S. life sciences companies...