February 13, 2018 at 02:50PM FDA Proposes to Require Electronic Submission of Certain Postmarketing Safety Reports for Approved New Animal Drugs

FDA proposed a rule to require animal drug sponsors to submit to the agency certain adverse drug experience and product manufacturing defect reports on Form FDA 1932 in electronic format.

via What's New: Animal & Veterinary http://ift.tt/2EoFhD5