COMMISSION IMPLEMENTING REGULATION (EU) 2025/2091 of 17 October 2025 laying down good manufacturing practice for veterinary medicinal products in accordance with Regulation (EU) 2019/6 of the European Parliament and of the Council ANNEX I STERILE PRODUCTS AND ASEPTIC MANUFACTURING ANNEX II BIOLOGICAL AND IMMUNOLOGICAL PRODUCTS ANNEX III SPECIFIC REQUIREMENTS FOR CERTAIN VETERINARY MEDICINAL PRODUCTS ANNEX IV COMPUTERISED SYSTEMS ANNEX V QUALIFICATION AND VALIDATION ANNEX VI TEMPLATE FOR THE SITE MASTER FILE Appendices ANNEX VII USE OF IONISING RADIATION IN THE MANUFACTURE OF VETERINARY MEDICINAL PRODUCTS ANNEX VIII ANNEX IX REAL TIME RELEASE TESTING AND PARAMETRIC RELEASE

COMMISSION IMPLEMENTING REGULATION (EU) 2025/2091 of 17 October 2025 laying down good manufacturing practice for veterinary medicinal products in accordance with Regulation (EU) 2019/6 of the European Parliament and of the Council ANNEX I STERILE PRODUCTS AND ASEPTIC MANUFACTURING ANNEX II BIOLOGICAL AND IMMUNOLOGICAL PRODUCTS ANNEX III SPECIFIC REQUIREMENTS FOR CERTAIN VETERINARY MEDICINAL PRODUCTS ANNEX IV COMPUTERISED SYSTEMS ANNEX V QUALIFICATION AND VALIDATION ANNEX VI TEMPLATE FOR THE SITE MASTER FILE Appendices ANNEX VII USE OF IONISING RADIATION IN THE MANUFACTURE OF VETERINARY MEDICINAL PRODUCTS ANNEX VIII ANNEX IX REAL TIME RELEASE TESTING AND PARAMETRIC RELEASEeu-regulation-2025-x-x-2091