Council Directive 92/27/EEC of 31 March 1992 on the labelling of medicinal products for human use and on package leaflets
Linked as:
Document options
Extract
Council Directive 92/27/EEC of 31 March 1992 on the labelling of medicinal products for human use and on package leaflets
No longer available (Autolink)
See the full content of this document
This document cites
- Council Directive 89/381/EEC of 14 June 1989 extending the scope of Directives 65/65/EEC and 75/319/EEC on the approximation of provisions laid down by Law, Regulation or Administrative Action relating to proprietary medicinal products and laying down special provisions for medicinal products derived from human blood or human plasma
- Council Directive 75/318/EEC of 20 May 1975 on the approximation of the laws of Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of proprietary medicinal products
- Council Directive 92/26/EEC of 31 March 1992 concerning the classification for the supply of medicinal products for human use
- Council Directive 65/65/EEC of 26 January 1965 on the approximation of provisions laid down by Law, Regulation or Administrative Action relating to proprietary medicinal products
- Council Directive 89/343/EEC of 3 May 1989 extending the scope of Directives 65/65/EEC and 75/319/EEC and laying down additional provisions for radiopharmaceuticals
