• the pharmaceutical authority of the veterinary pharmaceutical establishment manufacturer or operator upon authorisation of the marketing authorisation holder; 
• the marketing authorisation holder (MA) of the veterinary medicinal product.
   

• having a marketing authorisation valid in France on the day of application;
• with the exception of veterinary medicinal products which have obtained a marketing authorisation by the centralised procedure (apply to the European Agency in this case); 
• not having a marketing authorisation in France but manufactured in France (batch liberator).

• certificate of Origin – veterinary medicinal product without an MA  (CO Template in French (PDF)) 
• certificate of Origin and Free Sale (FSC Template in French (PDF)) 
• veterinary medicinal product certificate according to the WHO template (WHO Template in French (PDF))
• specific certificate for Taiwan (to be provided pre-completed, according to the template in force)
• the following may be provided in the annex, for medicinal products with an MA, on request
  • The complete SPC
  • The complete composition
  • The MA number 

• packaging and leaflet, if supplied;
• translation into English and/or Spanish of the complete SPC provided on company letterhead and in accordance with the French MA.

• bilingual French/English version by default;
• trilingual version (French/English/Spanish) on request.

Please note: WHO Model Certificates are issued in French/English only.

• only one by default unless otherwise stated;
• state the number of certificates requested;
• each certificate issued is identified with a unique number.

• a certified true copy of any administrative decisions relating to the applicant, the originals of which are held by ANSES-ANMV, in particular for information that is not included in the SPC (decision on MA or variation of MA, decision of authorisation of the manufacturing site responsible for batch release).