The Human Medicines (Amendment) Regulations 2016
1Citation and commencement
2Amendment of the Human Medicines Regulations 2012
3Amendment of regulation 8 (general interpretation)
4Amendment of regulation 18 (wholesale dealing in medicinal products)
5Amendment of regulation 20 (mixing of medicines)
6Amendment of regulation 43 (obligations of licence holder)
7Amendment of regulation 44 (requirement for wholesale dealers to deal only with specified persons)
8Amendment of regulation 213 (interpretation of Part 12)
9Amendment of regulation 214 (sale or supply of prescription only medicines)
10Amendment of regulation 223 (exemptions for doctors and dentists etc)
11Amendment of regulation 229 (exemption for supply by national health service bodies and local authorities)
12Amendment of regulation 248 (exemption for certain collection and delivery arrangements)
13Amendment of regulation 256A (interpretation of Part 12A)
14Amendment of regulation 256B (person who may sell medicinal products by information society services)
15Amendment of regulation 346 (Secretary of State to carry out a review of certain provisions)
16Amendment of Schedule 17 (exemption for sale, supply or administration by certain persons)
17Amendment of Schedule 23 (particulars in pharmacy records)

2016 No. 407

Medicines

The Human Medicines (Amendment) Regulations 2016

Made

Laid before Parliament

Coming into operation

The Secretary of State and the Minister for Health, Social Services and Public Safety make the following Regulations. They do so in the exercise of the powers conferred by section 2(2) and (5) of the European Communities Act 19721, having been designated for the purposes of section 2(2) of that Act in relation to medicinal products2.