OpenLegislation

Division 4 Identification and assay of adjuvantsF1

United Kingdom

Original text. Later amendments are not shown.

Insofar as testing procedures are available, the quantity and nature of the adjuvant and its components shall be verified on the finished product.

Annotations

Textual amendments

F1

Substituted by Commission Directive 2009/9/EC of 10 February 2009 amending Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to medicinal products for veterinary use (Text with EEA relevance).