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Division 3.2.2 Finished medicinal productF1

United Kingdom

Original text. Later amendments are not shown.

  1. 3.2.2.1Description and composition of the finished medicinal product
  2. 3.2.2.2Pharmaceutical development
  3. 3.2.2.3Manufacturing process of the finished medicinal product
  4. 3.2.2.4Control of excipients
  5. 3.2.2.5Control of the finished medicinal product
  6. 3.2.2.6Reference standards or materials
  7. 3.2.2.7Container and closure of the finished medicinal product
  8. 3.2.2.8Stability of the finished medicinal product

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).