SCHEDULE 2The manufacture of veterinary medicinal products

F1PART 2Authorisation of autogenous vaccines, blood-banks, stem cell centres and products manufactured under the cascade

Annotations:
Amendments (Textual)
F1

Sch. 2 Pt. 2 (paras. 14-25 entitled "Authorisation of autogenous vaccines, blood-banks, stem cell centres and products manufactured under the cascade") substituted for Sch. 2 Pt. 2 (paras. 14-19 entitled "Authorisation of manufacturers of autogenous vaccines"), Pt. 3 (paras. 20-24 entitled "Authorisation of blood banks"), Pt. 4 (paras. 25-29 entitled "Authorisation of manufacturers of products for administration under the cascade") and Pt. 5 (paras. 30-35 entitled "Authorisation of equine stem cell centres") (E.W.S.) (17.5.2024) by The Veterinary Medicines (Amendment etc.) Regulations 2024 (S.I. 2024/567), regs. 1(1), 92

F1Authorisation in relation to stem cellsE119

1

No person may collect stem cells for the purposes of treating animals other than a veterinary surgeon or a person acting under the responsibility of a veterinary surgeon.

2

No person may collect stem cells from embryonic tissues.

3

No person may administer any product grown from stem cells to a food-producing animal.

Annotations:
Extent Information
E1

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

Inspection of premisesE219

The Secretary of State must inspect the authorised premises, basing the frequency of the inspection on the risks associated with each premises’ history and the nature of the products handled at the premises.