PART 3

Veterinary medicines
CHAPTER 1

Regulations

Manufacture, marketing, supply and field trials
11
1
Regulations under section 10(1) may make provision about—
a
authorisations to manufacture veterinary medicines,
b
authorisations to import veterinary medicines,
c
authorisations to distribute veterinary medicines by way of wholesale dealing,
d
marketing authorisations,
e
marketing, importing or distributing active substances,
f
the categories of person who may supply veterinary medicines,
g
requirements that must be met in relation to the supply of veterinary medicines,
h
the registration of persons who supply or offer to supply veterinary medicines by means of the internet,
i
the circumstances in which veterinary medicines may be administered,
j
notification and reporting requirements in relation to veterinary medicines (or things purporting to be veterinary medicines) that have been placed on the market,
k
the labelling and packaging of veterinary medicines or the information that must be supplied with them or made available in relation to them,
l
advertising with regard to veterinary medicines, or
m
animal test certificates granted under the Veterinary Medicines Regulations 2013 (S.I. 2013/2033) for research purposes.
2
Regulations under section 10(1) may make provision corresponding or similar to provision in the following EU Regulations—
a
Regulation (EU) 2019/4 of the European Parliament and of the Council of 11 December 2018 on the manufacture, placing on the market and use of medicated feed, amending Regulation (EC) No 183/2005 of the European Parliament and of the Council and repealing Council Directive 90/167/EEC;
b
Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC.