OpenLegislation

Division 1.5 Specific requirements for different types of applicationsF1

United Kingdom

Original text. Later amendments are not shown.

Specific requirements for different types of applications are addressed in Part II of the present Annex.

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).