Part 8 Pharmacovigilance
United Kingdom
- 54Qualified persons responsible for pharmacovigilance
- 55Duties relating to the qualified person
- 56Adverse reactions to a veterinary medicinal product administered in the United Kingdom
- 57Adverse reactions to a veterinary medicinal product administered in a third country
- 58Periodic safety update reports
- 59Release of information by the marketing authorisation holder
- 60Action taken on account of pharmacovigilance