Paragraph 9 Adverse eventsF5 E1

England, Wales and Scotland

(1)

The F1manufacturer or importer of a veterinary medicinal product must—

(a)

notify the Secretary of State within 15 days of learning of any serious F2adverse events; and

(b)

make a record of each F3adverse event and serious adverse event on becoming aware of it and keep it for three years.

F4(2)

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Annotations

F1: Words in Sch. 6 para. 9 substituted (E.W.S.) (17.5.2024) by The Veterinary Medicines (Amendment etc.) Regulations 2024 (S.I. 2024/567), regs. 1(1), 159(a)
F2: Words in Sch. 6 para. 9(a) substituted (E.W.S.) (17.5.2024) by The Veterinary Medicines (Amendment etc.) Regulations 2024 (S.I. 2024/567), regs. 1(1), 159(b)
F3: Words in Sch. 6 para. 9(b) substituted (E.W.S.) (17.5.2024) by The Veterinary Medicines (Amendment etc.) Regulations 2024 (S.I. 2024/567), regs. 1(1), 159(c)
F4: Sch. 6 para. 9(2) omitted (E.W.S.) (17.5.2024) by virtue of The Veterinary Medicines (Amendment etc.) Regulations 2024 (S.I. 2024/567), regs. 1(1), 159(d)
F5: Words in Sch. 6 para. 9 heading substituted (E.W.S.) (17.5.2024) by The Veterinary Medicines (Amendment etc.) Regulations 2024 (S.I. 2024/567), regs. 1(1), 159(e)

E1: This version of this provision extends to England and Wales and Scotland only; a separate version has been created for Northern Ireland only