Grant etc of licences Grant etc of licences
- 17Manufacturing of medicinal products
- 17AManufacturing of MM medicinal products
- 17BManufacturing of POC medicinal products
- 18Wholesale dealing in medicinal products
- 18AApproved country for import
- 19Exemptions from requirement for wholesale dealer's licence
- 20Mixing of medicines
- 21Application for manufacturer's or wholesale dealer's licence
- 22Factors relevant to determination of application for manufacturer's or wholesale dealer's licence
- 23Grant or refusal of licence
- 24Standard provisions of licences
- 25Duration of licence
- 26General power to suspend, revoke or vary licences
- 27Procedure where licensing authority proposes to suspend, revoke or vary licence
- 27AEffect of suspension or variation relating to modular unit or POC site
- 28Suspension of licence in cases of urgency
- 29Variation of licence on the application of the holder
- 29AVariation of MM master file
- 29BVariation of POC master file
- 30Provision of information
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