Header
CAMEVET

CAMEVET Seminars

Introduction

Through annual meetings since 1992, CAMEVET focused on the harmonisation of the contents of technical outlines on biological and pharmacological products.

Following Seminars produced guidelines on Good Manufacturing Practices, templates for international approval certificates, and the organisation of the requirements for the registration of pharmaceutical and biological products under specific application forms.

Search & filter
All Filters
More filters Close filters
Cancel Confirm
Reset all filters

No results found

Please try again by changing the filter criteria or make sure your keywords are spelled correctly.