Regulation 21 Application for manufacturer's or wholesale dealer's licence

(1)

An application for a grant of a licence under this Part must—

(a)

be made to the licensing authority;

(b)

be made in the way and form specified in Schedule 3; and

(c)

contain or be accompanied by the information, documents, samples and other material specified in that Schedule.

(2)

An application must indicate the descriptions of medicinal products in respect of which the licence is required, either by specifying the descriptions of medicinal products in question or by way of an appropriate general classification.

Notes on Part 3

Textual amendments

F1: Pt. 3 heading and Pt. 3 Ch. 1 inserted (20.8.2013) by The Human Medicines (Amendment) Regulations 2013 (S.I. 2013/1855), regs. 1(1), 4

Notes on Chapter 2

Textual amendments

F1: Pt. 3 Ch. 2 heading inserted (20.8.2013) by The Human Medicines (Amendment) Regulations 2013 (S.I. 2013/1855), regs. 1(1), 4