Part 8 Pharmacovigilance
- 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