EMA Communication: Draft veterinary consultations
The European Medicines Agency has published the following reflection papers for consultation:
- Draft guideline for the demonstration of efficacy for veterinary medicinal products containing anticoccidial substances – Deadline 31 August 2019
- Draft guideline on requirements for the quality (production and control), safety and efficacy of allergen products for use in horses, dogs and cats – Deadline 31 August 2019
- Draft guideline on safety and residue data requirements for pharmaceutical veterinary medicinal products intended for minor use or minor species (MUMS)/limited market – Deadline 31 August 2019
For more information on the European regulatory system for medicines, please consult our brochure.