The Medicines for Human Use and Medical Devices (Fees Amendments) Regulations 2006 PDF Download
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Author: Great Britain
Publisher:
ISBN: 9780110741147
Category : Law
Languages : en
Pages : 12
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Book Description
Enabling power: European Communities Act 1972, s. 2 (2) & Finance Act 1973, s. 56 (1) (2) & Medicines Act 1971, s. 1 (1) (2). Issued: 03.03.2006. Made: 27.02.2006. Laid: 03.03.2006. Coming into force: 01.04.2006. Effect: S.I. 1994/105; 1995/449, 1116 amended. Territorial extent & classification: E/W/S/NI. General. Partially revoked by S.I. 2008/552 (ISBN 9780110810737)
Author: Great Britain
Publisher:
ISBN: 9780110741147
Category : Law
Languages : en
Pages : 12
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Book Description
Enabling power: European Communities Act 1972, s. 2 (2) & Finance Act 1973, s. 56 (1) (2) & Medicines Act 1971, s. 1 (1) (2). Issued: 03.03.2006. Made: 27.02.2006. Laid: 03.03.2006. Coming into force: 01.04.2006. Effect: S.I. 1994/105; 1995/449, 1116 amended. Territorial extent & classification: E/W/S/NI. General. Partially revoked by S.I. 2008/552 (ISBN 9780110810737)
Author: Great Britain
Publisher:
ISBN: 9780110759166
Category : Law
Languages : en
Pages : 20
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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: 07.03.2007. Made: 01.03.2007. Laid: 07.03.2007. Coming into force: 01.04.2007. Effect: S.I. 1994/105; 1995/449, 1116; 2002/618 amended. Territorial extent & classification: E/W/S/NI. General. Revoked by S.I. 2007/803(ISBN 9780110761398) in relation to England, Wales and Scotland. EC note: These Regs make amendments to reflect the amendment of Directive 2001/83/EC on the Community code relating to medicinal products by Regulation (EC) no. 1901/2006
Author: GREAT BRITAIN.
Publisher:
ISBN: 9780348246049
Category :
Languages : en
Pages : 0
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Book Description
Enabling power: Medicines and Medical Devices Act 2021, ss. 2 (1), 6 (1) (a). Issued: 14.03.2023. Sifted: -. Made: 09.03.2023. Laid: 10.03.2023. Coming into force: 01.04.2023. Effect: S.I. 2016/190 amended. Territorial extent & classification: E/W/S/NI. General
Author: Great Britain: Parliament: Merits of Statutory Instruments Committee
Publisher: Stationery Office/Tso
ISBN: 9780104850954
Category : Law
Languages : en
Pages : 9
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Book Description
27th report of Session 2005-06 : Drawing special attention to: Draft Information Sharing Index (England) Regulations 2006; Medicines for Human Use and Medical Devices (Fees Amendments) Regulations 2006; Commission for Social Care Inspection (Fees and Freq
Author: Great Britain
Publisher:
ISBN: 9780110749648
Category : Law
Languages : en
Pages : 8
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Book Description
Enabling power: Medicines Act 1971, s. 1 (1) (2). Issued: 01.08.2006. Made: 26.07.2006. Laid: 01.08.2006. Coming into force: 01.09.2006. Effect: S.I. 1994/105; 1995/1116 amended. Territorial extent & classification: E/W/S/NI. General. Partially revoked by S.I. 2008/552 (ISBN 9780110810737)
Author: Great Britain
Publisher:
ISBN: 9780110761398
Category : Law
Languages : en
Pages : 20
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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: 16.03.2007. Made: 12.03.2007. Laid: 16.03.2007. Coming into force: 13.03.2007 for reg. 14; 01.04.2007 for all other purposes. Effect: S.I. 1994/105; 1995/449, 1116; 2002/618 amended & 2007/610 revoked. Territorial extent & classification: E/W/S. General. Partially revoked by S.I. 2008/552 (ISBN 9780110810737). This Statutory Instrument has been made in consequence of a defect in SI 2007/610 (ISBN 9780110759166) and is being issued free of charge to all known recipients of that Statutory Instrument
Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 0309212456
Category : Medical
Languages : en
Pages : 318
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Book Description
Medical devices that are deemed to have a moderate risk to patients generally cannot go on the market until they are cleared through the FDA 510(k) process. In recent years, individuals and organizations have expressed concern that the 510(k) process is neither making safe and effective devices available to patients nor promoting innovation in the medical-device industry. Several high-profile mass-media reports and consumer-protection groups have profiled recognized or potential problems with medical devices cleared through the 510(k) clearance process. The medical-device industry and some patients have asserted that the process has become too burdensome and is delaying or stalling the entry of important new medical devices to the market. At the request of the FDA, the Institute of Medicine (IOM) examined the 510(k) process. Medical Devices and the Public's Health examines the current 510(k) clearance process and whether it optimally protects patients and promotes innovation in support of public health. It also identifies legislative, regulatory, or administrative changes that will achieve the goals of the 510(k) clearance process. Medical Devices and the Public's Health recommends that the U.S. Food and Drug Administration gather the information needed to develop a new regulatory framework to replace the 35-year-old 510(k) clearance process for medical devices. According to the report, the FDA's finite resources are best invested in developing an integrated premarket and postmarket regulatory framework.
Author: Great Britain
Publisher:
ISBN: 9780110488912
Category : Law
Languages : en
Pages : 12
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Book Description
Enabling power: European Communities Act 1972, s. 2 (2) & Finance Act, s. 56 (1) (2) & Medicines Act 1971, s. 1 (1) (2). Issued: 16.03.2004. Made: 10.03.2004. Laid: 10.03.2004. Coming into force: 01.04.2004. Effect: S.I. 1994/105; 1995/449, 1116 amended. Territorial extent & classification: E/W/S/NI. General. Partially revoked by S.I. 2008/552 (ISBN 9780110810737)
Author: Great Britain
Publisher:
ISBN: 9780110453248
Category :
Languages : en
Pages : 12
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Book Description
Enabling power: European Communities Act 1972, s. 2 (2) & Finance Act 1973 s. 56 (1) (2) & Medicines Act 1971 s. 1 (1) (2). Issued: 21.03.2003. Made: 11.03.2003. Laid: 11.03.2003. Coming into force: 01.04.2003 except for the purposes of reg. 4 (2) (3) (5) (b); 01.07.2003 for the purposes of reg. 4 (2) (3) (5) (b). Effect: S.I. 1994/105;1995/449, 1116 amended. Territorial extent & classification: UK. General. Partially revoked by S.I. 2008/552 (ISBN 9780110810737) and revoked by SI 2013/532 (ISBN 9780111536506)
Author: Tony White
Publisher: CRC Press
ISBN: 1315346397
Category : Medical
Languages : en
Pages : 337
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Book Description
Many doctors do not receive training early in their careers on the broad range of non-clinical aspects of their work, and confront day-to-day issues for which initial medical education has failed to prepare them. Experienced doctors and consultants can also experience a similar lack of accessible reference material on these aspects of their role and for the non-clinical training of their juniors. This book and its companion volume The Doctor's Handbook Part 1: managing your role beyond clinical medicine, have been written to address these and other needs. Previously published as The Specialist Registrar and New Consultant Handbook, these completely revised and reconfigured volumes reflect the changing everyday work of specialist trainees, registrars and consultants. Topics covered in Volume 2 include: *
