OpenLegislation

Title IX PHARMACOVIGILANCEF1

United Kingdom

Original text. Later amendments are not shown.

  1. 1General provisions
  2. 2Transparency and communications
  3. 3Recording, reporting and assessment of pharmacovigilance data
  4. 4Supervision of post-authorisation safety studies
  5. 5Implementation, Delegation and Guidance

Annotations

Textual amendments

F1

Substituted by Directive 2010/84/EU of the European Parliament and of the Council of 15 December 2010 amending, as regards pharmacovigilance, Directive 2001/83/EC on the Community code relating to medicinal products for human use (Text with EEA relevance).