- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Pwynt Penodol mewn Amser (01/05/2004)
- Gwreiddiol (Fel y'i Deddfwyd)
Version Superseded: 22/07/2004
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Medicines Act 1968, Section 37 is up to date with all changes known to be in force on or before 26 December 2024. There are changes that may be brought into force at a future date. Changes that have been made appear in the content and are referenced with annotations.
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(1)The provisions of sections F1...32, 34 and 36 of this Act shall have effect subject to the following provisions of this section.
(2)The restrictions imposed by [F2section 32] of this Act do not apply to anything done before the first appointed day, and the restrictions imposed by section 34 of this Act do not apply where the substance or article in question was administered before that day.
(3)Where, in the course of a series of investigations carried out during a period ending on the first appointed day,—
F3(a). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
(b)substances or articles have been administered by way of a medicinal test on animals,
the restrictions imposed by [F4section 32 of the Act do not apply to anything done] in relation to similar substances or articles for the purpose of continuing that series of investigations, if it is done on or after the first appointed day but before such date as may be appointed for the purposes of this section by an order made by the Ministers.
(4)If, on an application for F5... an animal test certificate which is made before the date appointed for the purposes of this section, it is proved to the reasonable satisfaction of the licensing authority that—
(a)[F6substances or articles specified in the application] were administered by way of a medicinal test on animals in the course of a series of investigations as mentioned in subsection (3) of this section, and
(b)that series of investigations was in progress immediately before the first appointed day, and
(c)the certificate is required for the purpose of continuing the series,
the applicant shall be entitled to the issue of a certificate such as will enable the series to be continued and completed within a reasonable time after the date appointed for the purposes of this section.
(5)Section 36(3) of this Act shall not have effect in relation to any application for a certificate as being a certificate to which the applicant is entitled by virtue of subsection (4) of this section; but the provisions of section 27 of this Act shall have effect in relation to any such application, as if—
(a)any reference in that section to a licence of right were a reference to such a certificate;
(b)for the reference in subsection (2)(a) of that section to the grounds of refusal therein mentioned there were substituted a reference to the grounds that the conditions specified in subsection (4) of this section have not been fulfilled in relation to the application; and
(c)in subsection (6) of that section the reference to sections 25 and 26 of this Act were a reference to subsection (4) of this section;
and for the purposes of the application of those provisions in accordance with this subsection the relevant date, in relation to any matters specified in the application, shall be the date appointed for the purposes of this section.
Textual Amendments
F1Word in s. 37(1) omitted (1.5.2004) by virtue of Medicines for Human Use (Clinical Trials) Regulations 2004 (S.I. 2004/1031), reg. 1, Sch. 10 para. 9(2)
F2Words in s. 37(2) substituted (1.5.2004) by Medicines for Human Use (Clinical Trials) Regulations 2004 (S.I. 2004/1031), reg. 1, Sch. 10 para. 9(3)
F3S. 37(3)(a) omitted (1.5.2004) by virtue of Medicines for Human Use (Clinical Trials) Regulations 2004 (S.I. 2004/1031), reg. 1, Sch. 10 para. 9(4)(a)
F4Words in s. 37(3) substituted (1.5.2004) by Medicines for Human Use (Clinical Trials) Regulations 2004 (S.I. 2004/1031), reg. 1, Sch. 10 para. 9(4)(b)
F5Words in s. 37(4) omitted (1.5.2004) by virtue of Medicines for Human Use (Clinical Trials) Regulations 2004 (S.I. 2004/1031), reg. 1, Sch. 10 para. 9(5)(a)
F6Words in s. 37(4)(a) substituted (1.5.2004) by Medicines for Human Use (Clinical Trials) Regulations 2004 (S.I. 2004/1031), reg. 1, Sch. 10 para. 9(5)(b)
Modifications etc. (not altering text)
C1Pt. II(ss. 6–50) extended with modifications by S.I. 1985/1403, art. 3(1)
C2Ss. 32-39 modified (1.1.1995) by S.I. 1994/3142, reg. 18(4)
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