PART 3F1Manufacture and distribution of medicinal products and active substances
Annotations:
Amendments (Textual)
F2CHAPTER 2Manufacturing and wholesale dealing
Annotations:
Amendments (Textual)
F2
Pt. 3 Ch. 2 heading inserted (20.8.2013) by The Human Medicines (Amendment) Regulations 2013 (S.I. 2013/1855), regs. 1(1), 4
Grant etc of licences
Application for manufacturer's or wholesale dealer's licence21
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.
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