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Guidance document is being distributed for comment purposes only. Objective is to standardize the data for submission of adverse events relating to veterinary medicinal products (VMPs) comments and suggestions regarding the document should be submitted to Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
Guidance document is being distributed for comment purposes only. Objective is to standardize the data for submission of adverse events relating to veterinary medicinal products (VMPs) comme…