Guideline

The following guideline can be ordered through the address listed in the "Source/Publisher"-category.
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NOTICE TO APPLICANTS Volume 6B VETERINARY MEDICINAL PRODUCTS Presentation and content of the dossier
Internet:	http://ec.europa.eu/enterprise/pharmaceuticals/eudralex/vol-6/b/vol6b_04_2004_final.pdf
Origin/Publisher:	EG-Kommission
Content:	Marketing Authorisation applications, which are to be submitted in either a national or Community procedure (i.e. to competent authorities of the Member States and the European Medicines Agency (EMEA), consist of administrative information and the necessary documentation to demonstrate the quality, safety and efficacy of the veterinary medicinal product. This applies to non-immunological and immunological veterinary medicinal products.
Status:	Notice to Applicants
Document Type:	Notice to Applicants