The Human Use Medicines Regulations 2012

The Human Use Medicines Regulations 2012 PDF Author: Great Britain
Publisher:
ISBN: 9780111527603
Category :
Languages : en
Pages : 318

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Book Description
Enabling power: European Communities Act 1972, s. 2 (2) (5) & Medicines Act 1968, ss. 87 (1), 88 (1) (2), 91 (2), 129 (1) (2) (5). Issued: 24.07.2012. Made: 19.07.2012. Laid: 24.07.2012. Coming into force: 14.08.2012. Effect: 1968 c.29, c.67; 1971 c.69; 1975 c.25; 1987 c.43; 1990 c.43; 1994 c.23; 1999 c.8; 2003 c.21; 2007 asp 113 & S.I. 1972/1265 (NI. 14); 1976/1213 (N.I. 22), 1214 (N.I. 23); 1978/1006; 1980/14; 1981/1115 (N.I. 22); 1986/1700, 1761; 1989/684; 1995/449; 1997/1830, 1997/2778 (N.I. 19), 2779 (N.I. 20); 2000/620; 2001/880, 1841, 3998; 2002/3170; 2003/1076, 1374, 1376, 1571, 1680; 2004/291, 478, 627, 1022, 1031, 1975; 2005/1478; 2007/121, 1523, 3544; 2008/548, 944, 1270, 3258 & S.S.I. 2004/115, 116; 2009/45, 183, 669; 2010/2880 & S.R. 1987/414; 1995/8; 1996/81; 1997/381; 1998/28, 45; 1999/433; 2001/422, 2002/1; 2003/34, 493; 2004/140; 2005/160, 161, 176; 2006/478; 2007/68, 234, 236 amended & S.I. 1973/367; 1976/968; 1978/40; 1983/1724; 1999/1129; 1992/605; 1993/834; 1994/105, 899, 1932, 1933, 3144; 1995/2321; 1996/482; 1997/1830; 1998/3105; 1999/267, 784; 2002/236; 2003/1618, 2317; 2004/480; 2005/765, 768, 1094, 1520, 1710, 2750, 2754, 2787, 2589; 2006/395, 1952; 2008/1692, 3097; 2009/1164, 3062; 2010/1882 revoked. Territorial extent & classification: E/W/S/NI. General. With correction slip dated November 2012. Revoked by SI 2013/1855 (ISBN 9780111102251)

The Human Use Medicines Regulations 2012

The Human Use Medicines Regulations 2012 PDF Author: Great Britain
Publisher:
ISBN: 9780111527603
Category :
Languages : en
Pages : 318

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Book Description
Enabling power: European Communities Act 1972, s. 2 (2) (5) & Medicines Act 1968, ss. 87 (1), 88 (1) (2), 91 (2), 129 (1) (2) (5). Issued: 24.07.2012. Made: 19.07.2012. Laid: 24.07.2012. Coming into force: 14.08.2012. Effect: 1968 c.29, c.67; 1971 c.69; 1975 c.25; 1987 c.43; 1990 c.43; 1994 c.23; 1999 c.8; 2003 c.21; 2007 asp 113 & S.I. 1972/1265 (NI. 14); 1976/1213 (N.I. 22), 1214 (N.I. 23); 1978/1006; 1980/14; 1981/1115 (N.I. 22); 1986/1700, 1761; 1989/684; 1995/449; 1997/1830, 1997/2778 (N.I. 19), 2779 (N.I. 20); 2000/620; 2001/880, 1841, 3998; 2002/3170; 2003/1076, 1374, 1376, 1571, 1680; 2004/291, 478, 627, 1022, 1031, 1975; 2005/1478; 2007/121, 1523, 3544; 2008/548, 944, 1270, 3258 & S.S.I. 2004/115, 116; 2009/45, 183, 669; 2010/2880 & S.R. 1987/414; 1995/8; 1996/81; 1997/381; 1998/28, 45; 1999/433; 2001/422, 2002/1; 2003/34, 493; 2004/140; 2005/160, 161, 176; 2006/478; 2007/68, 234, 236 amended & S.I. 1973/367; 1976/968; 1978/40; 1983/1724; 1999/1129; 1992/605; 1993/834; 1994/105, 899, 1932, 1933, 3144; 1995/2321; 1996/482; 1997/1830; 1998/3105; 1999/267, 784; 2002/236; 2003/1618, 2317; 2004/480; 2005/765, 768, 1094, 1520, 1710, 2750, 2754, 2787, 2589; 2006/395, 1952; 2008/1692, 3097; 2009/1164, 3062; 2010/1882 revoked. Territorial extent & classification: E/W/S/NI. General. With correction slip dated November 2012. Revoked by SI 2013/1855 (ISBN 9780111102251)

The Human Medicines Regulations 2012

The Human Medicines Regulations 2012 PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages : 0

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Book Description


Amendments to Human Medicines Regulations 2012

Amendments to Human Medicines Regulations 2012 PDF Author:
Publisher:
ISBN:
Category :
Languages : en
Pages :

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Pharmaceutical Medicine

Pharmaceutical Medicine PDF Author: Adrian Kilcoyne
Publisher: OUP Oxford
ISBN: 0191510394
Category : Medical
Languages : en
Pages : 473

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Book Description
The breadth of the pharmaceutical medicine can be daunting, but this book is designed to navigate a path through the speciality. Providing a broad overview of all topics relevant to the discipline of pharmaceutical medicine, it gives you the facts fast, in a user-friendly format, without having to dive through page upon page of dense text. With 136 chapters spread across 8 sections, the text offers a thorough grounding in issues ranging from medicines regulation to clinical trial design and data management. This makes it a useful revision aid for exams as well as giving you a taster of areas of pharmaceutical medicine adjacent to your current role. For healthcare professionals already working in the field, this book offers a guiding hand in difficult situations as well as supplying rapid access to the latest recommendations and guidelines. Written by authors with experience in the industry and drug regulation, this comprehensive and authoritative guide provides a shoulder to lean on throughout your pharmaceutical career.

The Human Medicines (Amendment) Regulations 2019

The Human Medicines (Amendment) Regulations 2019 PDF Author: GREAT BRITAIN.
Publisher:
ISBN: 9780111178782
Category :
Languages : en
Pages : 12

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Book Description
Enabling power: European Communities Act 1972, ss. 2 (2) (5). Issued: 24.01.2019. Sifted: -. Made: 14.01.2019. Laid: 18.01.2019. Coming into force: 09.02.2019. Effect: S.I. 2012/1916 amended. Territorial extent & classification: E/W/S/NI. General. EC note: These Regulations amend the Human Medicines Regulations 2012 in order to implement: points 8, 9, 11 and 12 of Article 1 of Directive 2011/62/EU of the European Parliament and of the Council of 8 June 2011 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use, as regards the prevention of the entry into the legal supply chain of falsified medicinal products (Directive 2011/62/EU); Commission Delegated Regulation (EU) 2016/161 of 2 October 2015 supplementing Directive 2001/83/EC of the European Parliament and of the Council by laying down detailed rules for the safety features appearing on the packaging of medicinal products for human use (the Delegated Regulation).

The Medicines (Products for Human Use) (Fees) (Amendment) Regulations 2012

The Medicines (Products for Human Use) (Fees) (Amendment) Regulations 2012 PDF Author: Great Britain
Publisher:
ISBN: 9780111529171
Category :
Languages : en
Pages : 4

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Book Description
Enabling power: Medicines Act 1971, s. 1 (1) & European Communities Act 1972, s. 2 (2) & Finance Act 1973, s. 56 (1) (2). Issued: 10.10.2012. Made: 04.10.2012. Laid: 10.10.2012. Coming into force: 02.11.2012. Effect: S.I. 2012/504 amended. Territorial extent & classification: E/W/S/NI. General

To Err Is Human

To Err Is Human PDF Author: Institute of Medicine
Publisher: National Academies Press
ISBN: 0309068371
Category : Medical
Languages : en
Pages : 312

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Book Description
Experts estimate that as many as 98,000 people die in any given year from medical errors that occur in hospitals. That's more than die from motor vehicle accidents, breast cancer, or AIDSâ€"three causes that receive far more public attention. Indeed, more people die annually from medication errors than from workplace injuries. Add the financial cost to the human tragedy, and medical error easily rises to the top ranks of urgent, widespread public problems. To Err Is Human breaks the silence that has surrounded medical errors and their consequenceâ€"but not by pointing fingers at caring health care professionals who make honest mistakes. After all, to err is human. Instead, this book sets forth a national agendaâ€"with state and local implicationsâ€"for reducing medical errors and improving patient safety through the design of a safer health system. This volume reveals the often startling statistics of medical error and the disparity between the incidence of error and public perception of it, given many patients' expectations that the medical profession always performs perfectly. A careful examination is made of how the surrounding forces of legislation, regulation, and market activity influence the quality of care provided by health care organizations and then looks at their handling of medical mistakes. Using a detailed case study, the book reviews the current understanding of why these mistakes happen. A key theme is that legitimate liability concerns discourage reporting of errorsâ€"which begs the question, "How can we learn from our mistakes?" Balancing regulatory versus market-based initiatives and public versus private efforts, the Institute of Medicine presents wide-ranging recommendations for improving patient safety, in the areas of leadership, improved data collection and analysis, and development of effective systems at the level of direct patient care. To Err Is Human asserts that the problem is not bad people in health careâ€"it is that good people are working in bad systems that need to be made safer. Comprehensive and straightforward, this book offers a clear prescription for raising the level of patient safety in American health care. It also explains how patients themselves can influence the quality of care that they receive once they check into the hospital. This book will be vitally important to federal, state, and local health policy makers and regulators, health professional licensing officials, hospital administrators, medical educators and students, health caregivers, health journalists, patient advocatesâ€"as well as patients themselves. First in a series of publications from the Quality of Health Care in America, a project initiated by the Institute of Medicine

Medicines (Products for Human Use) (Fees) Regulations 2012

Medicines (Products for Human Use) (Fees) Regulations 2012 PDF Author: Northern Ireland
Publisher:
ISBN: 9780337987472
Category :
Languages : en
Pages : 78

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Book Description


Si 2010/504 Medicines/prods for Human Use

Si 2010/504 Medicines/prods for Human Use PDF Author:
Publisher:
ISBN: 9780111520697
Category :
Languages : en
Pages :

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Dale and Appelbe's Pharmacy and Medicines Law

Dale and Appelbe's Pharmacy and Medicines Law PDF Author: Gordon E. Appelbe
Publisher: Pharmaceutical Press
ISBN: 0853699895
Category : Law
Languages : en
Pages : 609

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Book Description
This tenth edition of Dale and Appelbe's Pharmacy and Medicines Law, previously Dale and Appelbe's Pharmacy Law and Ethics, is your definitive guide to law relating to pharmacy and medicine practice in Great Britain. It covers law and professional regulation that all pharmacy and medicine professionals need to know.