PART 3F1Manufacture and distribution of medicinal products and active substances

Annotations:
Amendments (Textual)
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

F2CHAPTER 2Manufacturing and wholesale dealing

Annotations:
Amendments (Textual)

Grant etc of licences

Mixing of medicines20

1

Regulation 17(1) (manufacturing of medicinal products) does not apply to the mixing of medicines by—

a

a nurse independent prescriber;

b

a pharmacist independent prescriber;

c

a supplementary prescriber, if the mixing of medicines forms part of the clinical management plan for an individual patient;

F3ca

physiotherapist independent prescriber;

cb

podiatrist independent prescriber;

F6cc

a therapeutic radiographer independent prescriber;

F9cd

a paramedic independent prescriber;

d

a person acting in accordance with the written directions of a—

i

doctor,

ii

dentist,

iii

nurse independent prescriber, F4...

F5iv

pharmacist independent prescriber,

v

physiotherapist independent prescriber, F7...

vi

podiatrist independent prescriber; or

F8vii

therapeutic radiographer independent prescriber; or

F10viii

paramedic independent prescriber; or

e

a person acting in accordance with the written directions of a supplementary prescriber, if the mixing of medicines forms part of the clinical management plan for an individual patient.

2

In this regulation “mixing of medicines” means the combining of two or more medicinal products together for the purposes of administering them to meet the needs of an individual patient.