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CVM GFI #214 (VICH GL35) Pharmacovigilance of Veterinary Medicinal Products Electronic Standards for Transfer of Data

The objective of this guidance is to provide recommended standards to construct a single Adverse Event Report electronic message to transmit GL42 contents to all member regions and Product Problem Reports to FDA for veterinary medicinal products.

EMA Relaunches Policy 0070 On Publication Of Clinical Data For Medicinal Products For Human Use - Healthcare

NAFDAC nabs 3 suspected food fraud syndicate, others

NAFDAC nabs 3 suspected food fraud syndicate, others
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