Modifications etc. (not altering text)
C1Pt. 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)
218.—(1) For the purposes of this Chapter, a prescription only medicine is not sold or supplied in accordance with a prescription given by an appropriate practitioner who is an EEA health professional unless the following conditions are met.
[F1(2) Condition A is that—
(a)the prescription is issued in a relevant European State except the United Kingdom; and
(b)the prescribing EEA health professional is legally entitled to issue a prescription of that kind in the country in which the prescription is issued.]
[F2(3) Condition B is that the prescription is signed in ink by the prescribing EEA health professional.]
(4) Condition C is that the prescription is written in ink or otherwise so as to be indelible.
[F3(5) Condition D is that the prescription contains—
(a)the patient’s—
(i)surname,
(ii)first names written out in full, and
(iii)date of birth;
(b)the issue date of the prescription;
(c)the prescribing EEA health professional’s—
(i)surname,
(ii)first names written out in full,
(iii)professional qualification,
(iv)direct contact details including—
(aa)email address, and
(bb)telephone or fax number with the appropriate international prefix,
(v)work address, and
(vi)name of the relevant member State in which that EEA health professional works; and
(d)details about the prescribed product, including where applicable the—
(i)common name of the product,
(ii)brand name if—
(aa)the prescribed product is a biological medicinal product, or
(bb)the prescribing EEA health professional deems it medically necessary for that product to be dispensed and the EEA health professional’s reasons justifying the use of the branded product,
(iii)pharmaceutical formulation (tablet, solution, etc.),
(iv)quantity,
(v)strength of the medicinal product as defined in Article 1 of the 2001 Directive, and
(vi)dosage regimen.]
(6) Condition E is that the prescription—
(a)is not dispensed after the end of the period of six months beginning with the date on which it is signed by the EEA health professional; or
(b)in the case of a repeatable prescription—
(i)it is not dispensed for the first time after the end of that period, and
(ii)it is dispensed in accordance with the directions contained in the prescription.
(7) Condition F is that, in the case of a repeatable prescription that does not specify the number of times it may be dispensed—
(a)it is not dispensed on more than two occasions; or
(b)in the case of a prescription for an oral contraceptive, it is not dispensed on more than six occasions or after the end of the period of six months beginning with the date on which it is signed by the EEA health professional.
(8) This regulation is subject to regulation [F4219A (electronic prescriptions: EEA health professionals)].
Textual Amendments
F1Reg. 218(2) substituted (E.W.S.) (1.10.2014) by The Human Medicines (Amendment) (No. 2) Regulations 2014 (S.I. 2014/1878), regs. 1, 23 and reg. 218(2) substituted (N.I.) (1.10.2014) by The Human Medicines (Amendment) (No. 2) Regulations 2014 (S.R. 2014/324), regs. 1(1), 23
F2Reg. 218(3) substituted (E.W.S.) (31.3.2014) by The Human Medicines (Amendment) Regulations 2014 (S.I. 2014/490), regs. 1(2), 7(3) and reg. 218(3) substituted (N.I.) (31.3.2014) by The Human Medicines (Amendment) Regulations 2014 (S.R. 2014/323), regs. 1(2), 7(3)
F3Reg. 218(5) substituted (E.W.S.) (31.3.2014) by The Human Medicines (Amendment) Regulations 2014 (S.I. 2014/490), regs. 1(2), 7(4) and reg. 218(5) substituted (N.I.) (31.3.2014) by The Human Medicines (Amendment) Regulations 2014 (S.R. 2014/323), regs. 1(2), 7(4)
F4Words in reg. 218(8) substituted (E.W.S.) (1.7.2015) by The Human Medicines (Amendment) (No. 2) Regulations 2015 (S.I. 2015/903), regs. 1, 3 and words in reg. 218(8) substituted (N.I.) (1.7.2015) by The Human Medicines (Amendment) (No. 2) Regulations 2015 (S.R. 2015/259), regs. 1, 3