OpenLegislation

Division (2) F1

United Kingdom

Original text. Later amendments are not shown.

Two main sets of information shall be provided, dealing with the active substance(s) and with the finished medicinal product, respectively.

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).