The Medicines (Products for Human Use-Fees) Regulations 2008

The Medicines (Products for Human Use-Fees) Regulations 2008 PDF Author: Great Britain
Publisher:
ISBN: 9780110810737
Category : Law
Languages : en
Pages : 64

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Book Description
Enabling power: Medicines Act 1971, s. 1 (1) (2) & European Communities Act 1972, s. 2 (2) & Finance Act 1973, s. 56 (1) (2). Issued: 07.03.2008. Made: 28.02.2008. Laid: 07.03.2008. Coming into force: 01.04.2008. Effect: S.I. 1994/105 amended & S.I. 1998/574; 2000/592; 2001/795; 2002/236, 542; 2003/625; 2004/666; 2006/494, 2125; 2007/803 partially revoked & S.I. 1995/1116; 1996/683; 2000/3031; 2004/1157; 2005/1124, 2979 revoked. Territorial extent & classification: E/W/S/NI. General. Revoked by S.I. 2009/389 (ISBN 9780111474969) with savings. With correction slip dated March 2008

The Medicines (Products for Human Use-Fees) Regulations 2008

The Medicines (Products for Human Use-Fees) Regulations 2008 PDF Author: Great Britain
Publisher:
ISBN: 9780110810737
Category : Law
Languages : en
Pages : 64

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Book Description
Enabling power: Medicines Act 1971, s. 1 (1) (2) & European Communities Act 1972, s. 2 (2) & Finance Act 1973, s. 56 (1) (2). Issued: 07.03.2008. Made: 28.02.2008. Laid: 07.03.2008. Coming into force: 01.04.2008. Effect: S.I. 1994/105 amended & S.I. 1998/574; 2000/592; 2001/795; 2002/236, 542; 2003/625; 2004/666; 2006/494, 2125; 2007/803 partially revoked & S.I. 1995/1116; 1996/683; 2000/3031; 2004/1157; 2005/1124, 2979 revoked. Territorial extent & classification: E/W/S/NI. General. Revoked by S.I. 2009/389 (ISBN 9780111474969) with savings. With correction slip dated March 2008

The Medicines (Products for Human Use) (Fees) Regulations 2009

The Medicines (Products for Human Use) (Fees) Regulations 2009 PDF Author: Great Britain
Publisher:
ISBN: 9780111474969
Category : Law
Languages : en
Pages : 72

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Book Description
Enabling power: Medicines Act 1971, s. 1 (1) (2) & European Communities Act 1972, s. 2 (2) & Finance Act 1973, s. 56 (1) (2). Issued: 05.03.2009. Made: 23.02.2009. Laid: 05.03.2009. Coming into force: 01.04.2009. Effect: S.I. 1994/105; 2003/2321 amended & S.I. 2008/552 revoked with savings. Territorial extent & classification: E/W/S/NI. General. Revoked by S.I. 2010/551 (ISBN 9780111494547) with savings

Medicines (Products for Human Use - Fees) Regulations 1995

Medicines (Products for Human Use - Fees) Regulations 1995 PDF Author: Great Britain
Publisher:
ISBN: 9780110528786
Category : Drugs
Languages : en
Pages : 33

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Book Description
Medicines (Products for Human Use - Fees) Regulations 1995

The Medicines for Human Use (Marketing Authorisations Etc. ) Amendment Regulations 2008

The Medicines for Human Use (Marketing Authorisations Etc. ) Amendment Regulations 2008 PDF Author: Great Britain
Publisher:
ISBN: 9780111470978
Category : Law
Languages : en
Pages : 8

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Book Description
Enabling power: European Communities Act 1972, s. 2 (2). Issued: 08.12.2008. Made: 03.12.2008. Laid: 08.12.2008. Coming into force: 29.12.2008. Effect: 1968 c. 67 & S.I. 1994/3144; 2008/1692 amended. Territorial extent & classification: E/W/S/NI. General. EC note: These Regulations give effect in the United Kingdom to Regulation No 1901/2006 on medicinal products for paediatric use and amending Regulation No 1768/92, Directive 2001/20/EC, Directive 2001/83/EC and Regulation No 726/2004, as amended by Regulation No 1902/2006 amending Regulation 1901/2006 on medicinal products for paediatric use (the Paediatric Regulation).

The Medicines for Human Use (Clinical Trials) and Blood Safety and Quality (Amendment) Regulations 2008

The Medicines for Human Use (Clinical Trials) and Blood Safety and Quality (Amendment) Regulations 2008 PDF Author: Great Britain
Publisher:
ISBN: 9780110813257
Category : Law
Languages : en
Pages : 8

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Book Description
Enabling power: European Communities Act 1972, s. 2 (2). Issued: 07.04.2008. Made: 31.03.2008. Laid: 07.04.2008. Coming into force: 01.05.2008. Effect: S.I. 2004/1031; 2005/50 amended. Territorial extent & classification: E/W/S/NI. General. EC note: These Regulations amend the Medicines for Human Use (Clinical Trials) Regulations 2004 (the Clinical Trials Regulations) which implement Directive 2001/20/EC on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use. This includes updating the definition of the Clinical Trials Directive and Directive 2001/83/EC respectively to take account of the subsequent amendment of those Directives by Community Regulations

The Medicines (Products for Human Use - Fees) Amendment Regulations 2000

The Medicines (Products for Human Use - Fees) Amendment Regulations 2000 PDF Author: Great Britain
Publisher:
ISBN: 9780110187754
Category :
Languages : en
Pages : 8

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Book Description
Enabling power: European Communities Act 1972 , s. 2 (2). Issued: 20.11.2000. Made: 09.11.2000. Laid: 10.11.2000. Coming into force: 01.12.2000. Effect: SI 1995/1116 amended. Territorial extent & classification:E/W/S/N.I. General. Revoked by S.I. 2008/552 (ISBN 9780110810737). EC note: Relates to a procedure laid down in Ch. III of EC Council DIR 75/319/EEC

Medicines (Products for Human Use-Fees) Amendment Regulations 1996

Medicines (Products for Human Use-Fees) Amendment Regulations 1996 PDF Author: Great Britain
Publisher:
ISBN: 9780110542638
Category : Drugs
Languages : en
Pages : 6

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Book Description
Medicines (Products for Human Use-Fees) Amendment Regulations 1996

Regulating Medicines in a Globalized World

Regulating Medicines in a Globalized World PDF Author: National Academies of Sciences, Engineering, and Medicine
Publisher: National Academies Press
ISBN: 0309498635
Category : Medical
Languages : en
Pages : 169

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Book Description
Globalization is rapidly changing lives and industries around the world. Drug development, authorization, and regulatory supervision have become international endeavors, with most medicines becoming global commodities. Drug companies utilize global supply chains that often include facilities in countries with inconsistent regulations from those of the United States, perform pivotal trials in multiple countries to support registration submissions in various jurisdictions, and subsequently market their medicines throughout most of the world. These companies operate across borders and require individual national regulators to ensure that drugs authorized for use in their countries are safe and effective, and appropriate for their health care system and their population. This process involves significant resources and often duplicative work. It is important to consider how this process can be improved in order to better allocate resources, time, and efforts to improve public health. Regulating Medicines in a Globalized World: The Need for Increased Reliance Among Regulators considers the role of mutual recognition and other reliance activities among regulators in contributing to enhancing public health. This report identifies opportunities for leveraging reliance activities more broadly in order to potentially impact public health globally. Key topics in this report include the job of medicines regulators in today's world, what policy makers need to know about today's regulatory environment, stakeholder views of recognition and reliance, as well as removing impediments and facilitating action for greater recognition and reliance among regulatory authorities.

Current Law

Current Law PDF Author: Sweet & Maxwell, Limited
Publisher:
ISBN: 9781847037602
Category : Law
Languages : en
Pages : 682

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Book Description
The perfect combination - these two books together form a complete suite of upstream oil and gas agreements.

Statutory Instruments

Statutory Instruments PDF Author: Great Britain
Publisher:
ISBN:
Category : Delegated legislation
Languages : en
Pages : 1188

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Book Description