OpenLegislation

Division 1 MODULE 1: ADMINISTRATIVE INFORMATIONF1

United Kingdom

Original text. Later amendments are not shown.

  1. 1.1Table of contents
  2. 1.2Application form
  3. 1.3Summary of product characteristics, labelling and package leaflet
  4. 1.4Information about the experts
  5. 1.5Specific requirements for different types of applications
  6. 1.6Environmental risk assessment

Annotations

Textual amendments

F1

Substituted by Commission directive 2003/63/EC of 25 June 2003 amending Directive 2001/83/EC of the European Parliament and of the Council on the Community code relating to medicinal products for human use (Text with EEA relevance).