What is Directive 2001/83/EC on medicinal products?

Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use

What is the EU directive 2004/27/EC?

Whereas of Directive 2004/27/EC: . (1) Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use, codified and consolidated in a single text the texts of Community legislation on medicinal products for human use, in the interests

What is the F5 directive 2010 84/eu?

Textual Amendments F5 Substituted by Directive 2010/84/EU of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance, Directive 2001/83/EC on the Community code relating to medicinal products for human use (Text with EEA relevance).

When did the Council Directive 80/836/euratom come into effect?

Account should also be taken of Council Directive 80/836/Euratom of 15 July 1980 amending the Directives laying down the basic safety standards for the health protection 4Directive 2001/83/EC of the European Parliament and of the Council of 6 November…

What is directive 2002/98/EC (human blood directive)?

This gap is to be filled by Directive 2002/98/EC (“Human Blood Directive”) 6. It contains provisions to ensure that blood and its components are of comparable quality and safety throughout the blood transfusion chain in all Member States.

When was the last time the EU directive was last amended?

(2) Opinion of the European Parliament of 3 July 2001 (not yet published in the Official Journal) and Council Decision of 27 September 2001. (3) OJ 22, 9.2.1965, p. 369/65. Directive as last amended by Directive 93/39/EEC (OJ L 214, 24.8.1993, p. 22). (4) OJ L 147, 9.6.1975, p.