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12 December 2013 EMA/CAMP/RICH/355996/2005 Committee for Medicinal Products for Veterinary Use (CAMP) RICH GL42: Pharmacovigilance: data elements for submission of adverse event reports (Airs) Adoption
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What is vich gl42 - european?
VICH GL42 - European is a guideline established by the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products (VICH) for the European region.
Who is required to file vich gl42 - european?
Manufacturers and sponsors of veterinary medicinal products in the European region are required to file VICH GL42 - European.
How to fill out vich gl42 - european?
The VICH GL42 - European guideline provides specific instructions on how to fill out the required documentation for veterinary medicinal products.
What is the purpose of vich gl42 - european?
The purpose of VICH GL42 - European is to harmonize the technical requirements for the registration of veterinary medicinal products in the European region.
What information must be reported on vich gl42 - european?
The VICH GL42 - European guideline outlines the specific information that must be reported, including data on the product's safety, quality, and efficacy.
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