Transparency (veterinary medicines)

The European Medicines Agency (EMA) publishes information on veterinary medicines at various stages of their lifecycles, including on post-authorisation changes.

EMA publishes redacted agendas and minutes of the Committee for Veterinary Medicinal Products (CVMP) since 2013.

The published agendas and minutes include information on the post-authorisation procedures discussed by the committee, whether or not the procedure is finalised. This covers:

The following information is also made publicly available:

  • CVMP press releases which are published on a monthly basis after each CVMP meeting;
  • CVMP monthly reports which are published on a monthly basis after each CVMP meeting;
  • CVMP summaries of opinions which are product-specific and published shortly after adoption of the relevant CVMP opinion;
  • EPARs, which are product-specific and updated upon completion of post-authorisation procedures;
  • EMA annual reports and work programmes.

More information:

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