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 …

VICH GL32 (Safety: Developmental Toxicity) October 2002 - For implementation in October 2003 (Except EU: later date) - Revision 1 of May 2004 Download GL32_st7-Rev.pdf

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 …

VICH information and organisational documents VICH Strategy Charter Conference Documents Training General training material

The VICH has been established under the auspices of the WOAH. WOAH provides support to VICH and encourages its member countries to take into consideration the VICH results by providing ongoing …

The VICH guidelines are publically available through the VICH website. They are also published on the websites of the regulatory authorities of the VICH members and observers.

VICH GL27: Guidance on Pre-Approval Information for Registration of New Veterinary Medicinal Products for Food Producing Animals with Respect to Antimicrobial Resistance

This Guideline has been developed by the appropriate VICH Expert Working Group and is subject to consultation by the parties, in accordance with the VICH Process.

The scope of the VICH program covers veterinary medicinal products, including pharmaceuticals, biologicals (vaccines and other biological products) and medicated premixes.

The VICH Steering Committee is the driver of the harmonisation process. The Steering Committee is the only structure that is empowered to take decisions such as selecting topics, releasing draft guidelines …