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Version Superseded: 14/08/2012
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Medicines Act 1968, Section 22A is up to date with all changes known to be in force on or before 18 November 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)If the applicant gives notice under section 21(11) or section 22(3) of his wish to appear before and be heard by a person appointed by the licensing authority, the authority shall—
(a)make that appointment; and
(b)arrange for the applicant to have an opportunity of appearing before that person.
(2)The person appointed—
(a)shall not be, or at any time have been, a member of—
(i)the Commission on Human Medicines or any of its Expert Advisory Groups,
(ii)the Medicines Commission formerly established under section 2 of this Act or any of its committees, or
(iii)a committee established under section 4 of this Act, or any sub-committee of such a committee; and
(b)shall not be an officer or servant of any Minister of the Crown.
(3)Subject to subsection (4) of this section, the applicant shall provide the person appointed with—
(a)a written summary of the oral representations he intends to make; and
(b)any documents on which he wishes to rely in support of those representations,
before the end of the period of three months beginning with the date of the notice referred to in subsection (1) of this section.
(4)If the applicant so requests, the person appointed may, after consulting the licensing authority, extend the time limit referred to in subsection (3) of this section, up to a maximum period of six months beginning with the date of the notice referred to in subsection (1) of this section.
(5)If the applicant fails to comply with the time limit in subsection (3) of this section, or, where he has been granted an extended time limit under subsection (4) of this section, that time limit—
(a)he may not appear before or be heard by the person appointed, and
(b)the licensing authority shall decide whether to grant or refuse the licence, or to grant it otherwise than in accordance with the application, and notify the applicant accordingly.
(6)The applicant may not submit any additional written representations or documents once the time limit has expired, except with the permission of the person appointed.
(7)At the hearing before the person appointed, both the applicant and the licensing authority may make representations.
(8)If the applicant so requests the hearing shall be in public.
(9)After the hearing—
(a)the person appointed shall provide a report to the licensing authority; and
(b)the licensing authority shall take the report into account and decide whether to grant or refuse the licence, or to grant it otherwise than in accordance with the application, or to confirm or alter their decision, as the case may be.
(10)The licensing authority shall then—
(a)notify the applicant of their decision;
(b)if the applicant so requests, provide the applicant with a copy of the report of the person appointed.]
Textual Amendments
F1Ss. 22, 22A substituted for s. 22 (30.10.2005) by Medicines (Advisory Bodies) Regulations 2005 (S.I. 2005/1094), reg. 1(1), Sch. 1 para. 3
Modifications etc. (not altering text)
C1S. 22A applied by SI 1992/605 Sch. (as amended) (30.10.2005) by Medicines (Advisory Bodies) (No.2) Regulations 2005 (S.I. 2005/2754), reg. 1(2)(b), Sch. 4 para. 6(a)
C2S. 22A excluded (30.10.2005) by Medicines (Advisory Bodies) (No.2) Regulations 2005 (S.I. 2005/2754), reg. 1(2)(b), Sch. 5 para. 19(3)(a)(i)
C3S. 22A(10)(b) applied by SI 1978/1006 reg. 7(3) (as substituted (30.10.2005) by Medicines (Advisory Bodies) (No.2) Regulations 2005 (S.I. 2005/2754), reg. 1(2)(b), Sch. 4 para. 3(b))
C4Ss. 22A(2)-(9) applied by SI 1978/1006 reg. 7(3) (as substituted (30.10.2005) by Medicines (Advisory Bodies) (No.2) Regulations 2005 (S.I. 2005/2754), reg. 1(2)(b), Sch. 4 para. 3(b))
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