Commission Directive 99/104/EC amending the Annex to Council Directive 81/852/EEC on the approximation of the laws of the Member States relating to analytical, pharmacotoxicological and clinical standards and protocols in respect of the testing of veterinary medicinal products.
Country
Type of law
Legislation
Abstract
The Annex to Directive 81/852/EC is amended by the Annex of this Directive. The new Annex establishes that the applicant must demonstrate that the veterinary medical product is manufactured in accordance with the Note for Guidance on minimising the risk of transmitting animal spongiform encephalopathy agents via veterinary medicinal products and its updates, published by the European Commission in Volume 7 of its publication "The rules governing medicinal products in the European Union".
Attached files
Web site
Date of text
Entry into force notes
This Directive shall enter into force on the third day following its publication in the Official Journal of the European Communities.
Repealed
Yes
Serial Imprint
CELEX-EUR Official Journal L 3, 6 January 2000, pp. 18-20.
Source language
English
Legislation status
repealed
Legislation Amendment
No
Implemented by