C1PART 12Dealings with medicinal products
CHAPTER 2Sale and supply of medicines
Prescription only medicines
Prescribing and administration by supplementary prescribers215
1
A supplementary prescriber (“S”) may not give a prescription for a prescription only medicine unless S meets conditions A and C.
2
A supplementary prescriber (“S”) may not—
a
parenterally administer a prescription only medicine; or
b
give directions for the parenteral administration of a prescription only medicine,
unless S meets conditions B and C.
3
Condition A is that S is acting in accordance with the terms of a clinical management plan that—
a
relates to the patient to whom the product is prescribed;
b
has effect when the prescription is given; and
c
includes the particulars specified in Schedule 14.
4
Condition B is that S is acting in accordance with the terms of a clinical management plan that—
a
relates to the patient to whom the product is, or is to be, administered;
b
has effect when the product is administered or (as the case may be) the direction is given; and
c
includes the particulars specified in Schedule 14.
5
Condition C is that S has access to health records that—
a
are the health records of the patient to whom the plan relates; and
b
are used by any doctor or dentist who is a party to the plan.
6
This regulation is subject to regulation 216.
7
In this regulation—
“clinical management plan” means a written plan (which may be amended from time to time) relating to the treatment of an individual patient agreed by—
- a
the patient to whom the plan relates;
- b
the doctor or dentist who is a party to the plan; and
- c
any supplementary prescriber who is to prescribe, give directions for administration or administer under the plan;
- a
“health record” has the meaning given by section 68(2) of the Data Protection Act 1998 M1.
Pt. 12 modified (E.W.) (1.10.2015) by The Nicotine Inhaling Products (Age of Sale and Proxy Purchasing) Regulations 2015 (S.I. 2015/895), regs. 1(3), 4(2)