Part 8 PharmacovigilanceF1
United Kingdom Repealed
- 55Qualified persons responsible for pharmacovigilance
- 56Duties relating to the qualified person
- 57Adverse reactions to a veterinary medicinal product administered in the United Kingdom
- 58Adverse reactions to a veterinary medicinal product administered in a third country
- 59Periodic safety update reports
- 60Release of information by the marketing authorisation holder
- 61Action taken on account of pharmacovigilance
Annotations
Textual amendments
- F1
Regulations revoked (except reg. 45(2)) (1.10.2009) by The Veterinary Medicines Regulations 2009 (S.I. 2009/2297), regs. 1, 45 (with reg. 3)