Commission Directive 91/507/EEC of 19 July 1991 modifying the Annex to Council Directive 75/318/EEC on the approximation of the laws of Member States relating to analytical, pharmacotoxicological and clinical standards and protocols in respect of the testing of medicinal products
- No longer in force
- CELEX number: 31991L0507
- Official Journal: JOL_1991_270_R_0032_025
- Form: Directive
- Procedure number: --
- Languages:
- da
- de
- el
- en
- fi
- fr
- it
- nl
- pt
- es
- sv
Dates
Date of document: - July 19, 1991
- September 26, 1991
- September 19, 1991
- Entry into force - Date notif.
- January 1, 1992
- At the latest See Art 2
- January 1, 1995
- At the latest See Art 2
- December 17, 2001
- See 31975L0318
Modified by
Corrected by:
- October 30, 1991 - 31991L0507R(01)
- November 22, 1991 - 31991L0507R(02)
Affected by case
Legal basis
- 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 89/342/EEC of 3 May 1989 extending the scope of Directives 65/65/EEC and 75/319/EEC and laying down additional provisions for immunological medicinal products consisting of vaccines, toxins or serums and allergens
- 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
- 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
EuroVoc Vocabulary
- Standard
- Pharmaceutical product
- Internal market - Principles
- Testing
- Public health
- Industry
- Technical barriers
- Proprietary medicinal products
- Approximation of laws