The Law on Medicines Volume 3 Distribution and Selling

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 patchwor...

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Bibliographic Details
Main Author: Harrison, H.S.
Format: eBook
Language:English
Published: Dordrecht Springer Netherlands 1986, 1986
Edition:1st ed. 1986
Subjects:
Online Access:
Collection: Springer Book Archives -2004 - Collection details see MPG.ReNa
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245 0 0 |a The Law on Medicines  |h Elektronische Ressource  |b Volume 3 Distribution and Selling  |c by H.S. Harrison 
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505 0 |a Division 5: Controls over Sale, Supply and Administration of Medicines -- III Further Provisions Relating to Dealings with Medicinal Products -- The Medicines (Administration of Radioactive Substances) Regulations 1978 -- The Medicines (Bal Jivan Chamcho Probition) (No.2) Order 1977 -- The Medicines (Prohibition of Non-medicinal Antimicrobial Substances) Order 1977 -- The Medicines (Chloroform Prohibition) Order 1979 as amended -- The Medicines (Phenacetin Prohibition) Order 1979 -- The Medicines (Stilbenes and Thyrostatic Substances Prohibition) Order 1982 -- Divison 6: Controls over Sale, Supply and Administration of Veterinary Products -- The Medicines (Restriction on the Administration of Veterinary Medicinal Products) Regulations 1983 -- The Medicines (Veterinary Drugs) (General Sale List) Order 1984 -- The Medicines (Veterinary Drugs) (Prescription Only) Order 1985 -- The Medicines (Exemptions from Restrictions on the Retail Sale or Supply of Veterinary Drugs) Order 1984 as amended -- Division 7: Quality of Medicines and Medicated Animal Feeding Stuffs -- VIII British Pharmacopoeia and other Publications -- II Certificate of Analysis or Examination of Animal Feeding Stuff (1) -- Division 8 Pharmacies -- IV Pharmacies 
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520 |a 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