VICH is a trilateral (EU-Japan-USA) programme aimed at harmonising technical requirements for veterinary product registration. Its full title is the International Cooperation on Harmonisation of Technical Requirements for Registration of Veterinary Medicinal Products. VICH was officially launched in April 1996. Questionnaire to regulatory authorities and to industry representatives in non-VICH countries (reply by August 15, 2009 please)     Overview of VICH structure The parties to VICH The Steering Committee Expert Working Groups and topic leaders Observers The OIE The VICH Secretariat (IFAH) The Driver : The Steering Commitee The 9-step procedure The official Organisational Charter Quality Safety Ecotoxicity Good Clinical Practice (GCP) Anthelmintics Pharmacovigilance Biologicals quality monitoring Antimicrobial resistance Target Animal Safety Summary table of VICH guidelines Official texts of final guidelines Official texts of draft guidelines VICH Guidelines by Category Documents in consultation             Steering Committee and Expert Working Groups Addresses Secretariat   Dates of next meetings Press releases / past meetings VICH statements   NVAL (Engish version) ECVAM - European Center for the Validation of Alternative Methods ECVAM Database Service "DB-ALM"