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- Draft FDA Guidance on Submission and Expedited Review of Abbreviated Laboratory Packages From Accredited Laboratories
Draft FDA Guidance on Submission and Expedited Review of Abbreviated Laboratory Packages From Accredited Laboratories
February 23, 2009, Covington E-Alert
August 5, 2020, Covington Alert
On Monday, FDA published for public comment a proposed rule concerning the submission of certain data elements for veterinary devices imported or offered for import via the Automated Commercial Environment (ACE) or other U.S. Customs and Border Protection (CBP)-authorized electronic data interchange (EDI) system.[1] Comments are due by October 19, 2020. The ...
January 26, 2009, Covington E-Alert
January 19, 2007, Covington E-Alert