The Medicines for Human Use (Manufacturing, Wholesale Dealing and Miscellaneous Amendments) Regulations 2005 PDF Download
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Author: Great Britain
Publisher:
ISBN: 9780110734453
Category : Law
Languages : en
Pages : 36
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Book Description
Enabling power: European Communities Act 1972, s. 2 (2) & Medicines Act 1968, ss. 18 (1), 47 (1), 129 (1) (5). Issued: 03.11.2005. Made: 10.10.2005. Laid: 10.10.2005. Coming into force: 30.10.2005. Effect: 1968 c. 67; S.I. 1971/972, 974; 1974/832; 1977/2130 amended. Territorial extent & classification: E/W/S/NI. General. EC note: These Regs implement certain provisions of Directive 2004/27/EC amending Directive 2001/83/EC on the Community code for medicinal products for human use, make changes to certain existing provisions which implement Directive 2001/83/EC and make consequential amendments to various enactments. With correction slip, dated March 2006
Author: Great Britain
Publisher:
ISBN: 9780110734453
Category : Law
Languages : en
Pages : 36
Get Book Here
Book Description
Enabling power: European Communities Act 1972, s. 2 (2) & Medicines Act 1968, ss. 18 (1), 47 (1), 129 (1) (5). Issued: 03.11.2005. Made: 10.10.2005. Laid: 10.10.2005. Coming into force: 30.10.2005. Effect: 1968 c. 67; S.I. 1971/972, 974; 1974/832; 1977/2130 amended. Territorial extent & classification: E/W/S/NI. General. EC note: These Regs implement certain provisions of Directive 2004/27/EC amending Directive 2001/83/EC on the Community code for medicinal products for human use, make changes to certain existing provisions which implement Directive 2001/83/EC and make consequential amendments to various enactments. With correction slip, dated March 2006
Author: John P. Griffin
Publisher: John Wiley & Sons
ISBN: 9781444317565
Category : Business & Economics
Languages : en
Pages : 776
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Book Description
The Textbook of Pharmaceutical Medicine is a standardreference for all those working in pharmaceutical medicine and therecognised text for the UK Faculty of Pharmaceutical MedicineDiploma. This is a comprehensive volume covering the processes bywhich medicines are developed, tested and approved. Regulations fordrug development in the UK, EU, USA, Australia and Japan arediscussed, providing relevant information for drug approval in themain continents where new drugs are developed. The chapters are written by leading academics, medical directorsand lawyers, providing authoritative and in-depth information fortrainees on the Faculty course, and for physicians working in thepharmaceutical industry. As well as thorough updating of theregulatory chapters, the 6th edition includes chapters onthese vital new areas: Paediatric regulation Ethics Due diligence and the pharmaceutical physician
Author: Ian Kennedy
Publisher: Oxford University Press, USA
ISBN: 0199544409
Category : Language Arts & Disciplines
Languages : en
Pages : 1317
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Book Description
Replete with references to primary sources and the secondary literature, this major undertaking provides a comprehensive exposition of English medical law, from the organization of health care to the legal meaning of death.
Author: Great Britain: Parliament: Merits of Statutory Instruments Committee
Publisher: The Stationery Office
ISBN: 9780104008416
Category : Political Science
Languages : en
Pages : 232
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Book Description
management of secondary Legislation : 29th report of session 2005-06, Vol. 2: Evidence
Author: British Medical Association
Publisher: John Wiley & Sons
ISBN: 1444355643
Category : Medical
Languages : en
Pages : 919
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Book Description
This is your source for authoritative and comprehensive guidance from the British Medical Association (BMA) Medical Ethics Department covering both routine and highly contentious medico-legal issues faced by health care professionals. The new edition updates the information from both the legal and ethical perspectives and reflects developments surrounding The Mental Capacity Act, Human Tissue Act, and revision of the Human Fertilisation and Embryology Act.
Author: Great Britain
Publisher:
ISBN:
Category : Delegated legislation
Languages : en
Pages : 980
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Book Description
Author: Great Britain
Publisher:
ISBN:
Category : Delegated legislation
Languages : en
Pages : 512
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Book Description
Author: Catherine Hare
Publisher: Routledge
ISBN: 1135475806
Category : Business & Economics
Languages : en
Pages : 190
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Book Description
A practical approach to developing and operating an effective programme to manage hybrid records within an organization. This title positions records management as an integral business function linked to the organization's business aims and objectives. The authors also address the records requirements of new and significant pieces of legislation, such as data protection and freedom of information, as well as exploring strategies for managing electronic records. Bullet points, checklists and examples assist the reader throughout, making this a one-stop resource for information in this area.
Author: Great Britain
Publisher:
ISBN:
Category : Law
Languages : en
Pages : 1512
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Book Description
Author: Vanessa Plate
Publisher: Columbia University Press
ISBN: 3838201353
Category : Law
Languages : en
Pages : 176
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Book Description
In times of situational therapeutic impasse, health care professionals (HCPs) are under pressure to conduct off-label, unlicensed and compassionate drug use—generally summarized under the term non-licensed drug use (NDU). Liability, contractual and penal risks pose a problem when treating a patient in a non-licensed way. There is a knowledge gap about institutional and governmental methods to resolve these problems. Different countries have developed strategies to manage NDU. Vanessa Platé gives a comprehensive overview of practices Canada, the U.S., the U.K., Japan, France, Germany, Switzerland, Austria, and the transnational E.U. A must-read for everyone interested in the discussion on how to administer the best treatment, especially regarding early access to yet unapproved treatments.
