Medicines (Standard Provisions for Licences and Certificates) Amendment (No. 3) Regulations 1977 PDF Download
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Languages : en
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Author: Great Britain
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ISBN: 9780110710532
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Languages : en
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Enabling power: Medicines act, 1968, s.47(1). Issued: 5.7.77. Made: 21.6.77. Laid: 24.6.77. Coming into force: 15.7.77. Effect: S.I. 1971/972, amended.
Author: Great Britain
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ISBN: 9780110706757
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Languages : en
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Enabling power: Medicines act, 1968, s.47(1). Issued: 21.4.77. Made: 6.4.77. Laid: 21.4.77. Coming into force: 12.5.77. Effect: S.I. 1971/972, amended.
Author: Great Britain
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ISBN: 9780110710396
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Languages : en
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Enabling power: Medicines act, 1968, s.47(1). Issued: 6.7.77. Made: 16.6.77. Laid: 23.6.77. Coming into force: 14.7.77. Effect: S.I. 1971/972, amended.
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Languages : en
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Author: Great Britain
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ISBN: 9780110710518
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Languages : en
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Enabling power: Medicines act, 1968, ss.18(1), 36(1). Issued: 5.7.77. Made: 21.6.77. Laid: 24.6.77. Coming into force: 15.7.77. Effect: S.I. 1971/ 973, amended.
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Author: H.S. Harrison
Publisher: Springer Science & Business Media
ISBN: 9401098581
Category : Law
Languages : en
Pages : 544
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Book Description
The Medicines Act 1968 together with its delegated legislation comprehensively controls the manufacture, packaging, labelling, distribution and promotion of medicines for both human and animal use in the United Kingdom. It also controls the import and export of such medicines. It replaced a patchwork of controls which evolved over a century. Since its enactment, more than 150 items of delegated legislation (orders and regulations) have been made under its provisions and about 130 are still operative. The sheer physical bulk of this mass of material causes difficulty, not only in comprehension but also in finding the detail so often required. The situation is exacerbated by the fact that some pieces of legislation have been amended several times. My principal aim is to provide a reference book which contains all of the provisions of the Act and its various orders, regulations as amended to date. The material is arranged to facilitate the search for detail. In order to assist the reader in finding his way through this maze, Chaper 1 consists of a survey of the situation which existed before the Act came into being, together with a synopsis of the present controls. This should enable the reader to appreciate the changes which have occurred and how the system works.
Author: Great Britain
Publisher:
ISBN: 9780110494494
Category : Law
Languages : en
Pages : 4
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Enabling power: Medicines Act 1968, ss. 47 (1), 129 (5). Issued: 07.07.2004. Made: 30.06.2004. Laid: 07.07.2004. Coming into force: 30.07.2004. Effect: S.I. 1971/972 amended. Territorial extent & classification: E/W/S/NI. General. EC note: These Regs. implement provisions in DIR 2001/83/EC, which relate to the definition of "good manufacturing practice", and so implement DIR 2003/94/EC, in so far as that Directive relates to the manufacture of medicinal products for human use, other than "investigational medicinal products" (products used in clinical trial).
