- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Pwynt Penodol mewn Amser (03/12/2007)
- Gwreiddiol (a wnaed Fel)
Version Superseded: 01/04/2008
Point in time view as at 03/12/2007. This version of this provision has been superseded.
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There are currently no known outstanding effects for the The Prescription Only Medicines (Human Use) Order 1997, Section 3B.
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3B.—(1) Subject to paragraph (2), a supplementary prescriber may—
(a)give a prescription for a medicinal product referred to in article 3; or
(b)if that medicinal product is for parenteral administration—
(i)administer that medicinal product, or
(ii)give directions for the administration of that medicinal product,
only where he complies with the conditions as to the cases or circumstances in which he may do so specified in paragraph (3).
(2) Paragraph (1) does not apply if—
(a)the supplementary prescriber is a [F2community practitioner nurse prescriber] and the medicinal product prescribed or administered, or in respect of which he gives directions for administration, falls within a description or class of medicinal products specified in Schedule 3; or
(b)the supplementary prescriber is [F3a nurse independent prescriber] and—
(i)the medicinal product prescribed or administered, or in respect of which he gives directions for administration, falls within a description or class of medicinal products specified in article 3A(1), and
(ii)he satisfies any applicable condition specified by virtue of article 3A(3) [F4; and]
[F5(c)the supplementary prescriber is a pharmacist independent prescriber and the medicinal product prescribed or administered, or in respect of which he gives directions for administration—
(i)is a prescription only medicine, and
(ii)is not a controlled drug.]
(3) The conditions referred to in paragraph (1) are that—
(a)the supplementary prescriber is acting in accordance with the terms of a clinical management plan which—
(i)relates to the patient for whom the product is prescribed or to whom it is, or is to be, administered,
(ii)is in effect at the time the prescription or direction is given or, as the case may be, the product is administered, and
(iii)includes the particulars specified in Schedule 3B;
F6(b). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(c)the supplementary prescriber has access to the health records of the patient to whom the plan relates which are used by any doctor or dentist who is a party to the plan.]
Textual Amendments
F1Arts. 3B, 3C inserted (4.4.2003) by The Prescription Only Medicines (Human Use) Amendment Order 2003 (S.I. 2003/696), arts. 1(1), 6
F2Words in art. 3B(2)(a) substituted (1.5.2006) by The Medicines for Human Use (Prescribing) (Miscellaneous Amendments) Order 2006 (S.I. 2006/915), arts. 1(1), 5(a)
F3Words in art. 3B(2)(b) substituted (1.5.2006) by The Medicines for Human Use (Prescribing) (Miscellaneous Amendments) Order 2006 (S.I. 2006/915), arts. 1(1), 5(b)(i)
F4Word in art. 3B(2)(b)(ii) inserted (1.5.2006) by The Medicines for Human Use (Prescribing) (Miscellaneous Amendments) Order 2006 (S.I. 2006/915), arts. 1(1), 5(b)(ii)
F5Art. 3B(2)(c) inserted (1.5.2006) by The Medicines for Human Use (Prescribing) (Miscellaneous Amendments) Order 2006 (S.I. 2006/915), arts. 1(1), 5(c)
F6Art. 3B(3)(b) omitted (7.4.2005) by virtue of The Medicines for Human Use (Prescribing) Order 2005 (S.I. 2005/765), arts. 1(1), 4
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