The Medicines for Human Use (Clinical Trials) Amendment Regulations 2006 PDF Download
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Author: Great Britain
Publisher:
ISBN: 9780110748610
Category : Drugs
Languages : en
Pages : 12
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Book Description
Enabling power: European Communities Act 1972, s. 2 (2). Issued: 20.07.2006. Made: 13.07.2006. Laid: 20.07.2006. Coming into force: 29.08.2006. Effect: S.I. 2004/1031 amended. Territorial extent & classification: E/W/S/NI. General. EC note: These Regulations amend the Medicines for Human Use (Clinical Trials) Regulations 2004 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 in human use. In particular, they implement Commission Directive 2005/28/EC laying down principles and detailed guidelines for good clinical practice as regards investigational medicinal products for human use, as well as the requirements for authorisation of the manufacturing or importation of such products (the GCP Directive) and make other miscellaneous amendments
Author: Great Britain
Publisher:
ISBN: 9780110748610
Category : Drugs
Languages : en
Pages : 12
Get Book Here
Book Description
Enabling power: European Communities Act 1972, s. 2 (2). Issued: 20.07.2006. Made: 13.07.2006. Laid: 20.07.2006. Coming into force: 29.08.2006. Effect: S.I. 2004/1031 amended. Territorial extent & classification: E/W/S/NI. General. EC note: These Regulations amend the Medicines for Human Use (Clinical Trials) Regulations 2004 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 in human use. In particular, they implement Commission Directive 2005/28/EC laying down principles and detailed guidelines for good clinical practice as regards investigational medicinal products for human use, as well as the requirements for authorisation of the manufacturing or importation of such products (the GCP Directive) and make other miscellaneous amendments
Author: Great Britain
Publisher:
ISBN: 9780110753287
Category : Drugs
Languages : en
Pages : 4
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Book Description
Enabling power: European Communities Act 1972, s. 2 (2). Issued: 21.11.2006. Made: 15.11.2006. Laid: 21.11.2006. Coming into force: 12.12.2006. Effect: S.I. 2004/1031 amended. Territorial extent & classification: E/W/S/NI. General. EC note: These Regulations amend the Medicines for Human Use (Clinical Trials) Regulations 2004 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 in human use
Author: Tony White
Publisher: Radcliffe Publishing
ISBN: 1846194598
Category : Medical
Languages : en
Pages : 333
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Book Description
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. The two volumes of The Doctors Handbook are an essential reference for all doctors, from specialist trainees to consultants.
Author: Tony White
Publisher: CRC Press
ISBN: 1315357615
Category : Medical
Languages : en
Pages : 198
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Book Description
To maximise the effectiveness of their work, NHS employees need a clear understanding of the structures and systems of the organisation in which they work. However, this information can be widely spread, hard to access and difficult to gain a working overview of, and the pace of changes and initiatives can seem almost dizzying. This book draws together a clear picture of the modern NHS, from funding and governance to reports, inquiries and overarching legislation. The book is clear and easy to understand and crucially includes full references to provide a one-stop point of access to the most detailed and up-to-date information available. This book is essential reading for workers in the NHS at all levels, including managers, administrators and clinical professionals. It is vital reading for managers and staff at commercial companies working with the NHS. It will also be of interest to campaigners, patient interest groups, researchers and journalists with an interest in the NHS. Specialty registrars and consultants can also find the information from the book, and much more, in The Doctor's Handbook Parts 1 & 2, by the same author. 'Rather than long narrative histories or complex explanations, the author signposts readers to sources of further information, making this book the quick guide so many of us need' - from the Foreword by Sir Ian Carruthers
Author: Philip Wiffen
Publisher: Oxford University Press
ISBN: 0191054704
Category : Medical
Languages : en
Pages : 618
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Book Description
Complementing the guidelines in the British National Formulary, the third edition of the Oxford Handbook of Clinical Pharmacy remains the indispensable guide to clinical pharmacy, providing all the information needed for practising and student pharmacists. It presents handy practical guidance in a quick-reference, bullet-point format to give the reader the knowledge and confidence needed to provide a clinical pharmacy service. Including key information on controlled drugs, adverse drug reactions, interactions, communication skills, and confidentiality, this extensively revised addition to the bestselling Oxford Handbook series is the fundamental pharmacy reference tool. It features chapters on adherence, anaphylaxis, clinical trials, herbal medicines, palliative care, patient management, pharmaceutical calculations, research, policy, and therapy related issues. Thoroughly revised and updated, the Oxford Handbook of Clinical Pharmacy includes brand new topics, including content on health coaching, residency and on-call, HIV and TB and mental health.
Author: Sumantra Ray
Publisher: Oxford University Press
ISBN: 0191502952
Category : Medical
Languages : en
Pages : 603
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Book Description
The Oxford Handbook of Clinical and Healthcare Research is an evidence-based, succinct, and easy-to-use reference for the full range of clinical and healthcare research topics. Providing a wide breadth of essential knowledge, this comprehensive text takes the researcher through the steps from general good clinical practice in healthcare research to the process and management of research. This handbook includes clear instructions on the legislative and practical requirements of commissioning, conducting, analysing, and reporting research for those in clinical or healthcare practice, education, or training. Written with Good Clinical Practice (GCP) education in mind, it includes valuable information needed for the accredited certificates and diploma-level benchmark exams now commonly required by employers. This is a definitive text for all clinical and healthcare research students, as well as graduates with an interest in clinical and healthcare research.
Author: Emma Cave
Publisher: Manchester University Press
ISBN: 1526157152
Category : Law
Languages : en
Pages : 729
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Book Description
Embryo research, cloning, assisted conception, neonatal care, pandemic vaccine development, saviour siblings, organ transplants, drug trials – modern developments have transformed the field of medicine almost beyond recognition in recent decades and the law struggles to keep up. In this highly acclaimed and very accessible book Margaret Brazier, Emma Cave and Rob Heywood provide an incisive survey of the legal situation in areas as diverse as fertility treatment, patient consent, assisted dying, malpractice and medical privacy. The seventh edition of this book has been fully revised and updated to cover the latest cases, Brexit-related regulatory reform and COVID-19 pandemic measures. Essential reading for healthcare professionals, lecturers, medical and law students, this book is of relevance to all whose perusal of the daily news causes wonder, hope and consternation at the advances and limitations of medicine, patients and the law.
Author: Phil Wiffen
Publisher: Oxford University Press, USA
ISBN: 0199603642
Category : Medical
Languages : en
Pages : 696
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Book Description
This handbook is the definitive quick reference guide to clinical pharmacy, providing practising and student pharmacists with a wealth of practical information.
Author: Divya Vohora
Publisher: Academic Press
ISBN: 0128020989
Category : Medical
Languages : en
Pages : 527
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Book Description
Pharmaceutical Medicine and Translational Clinical Research covers clinical testing of medicines and the translation of pharmaceutical drug research into new medicines, also focusing on the need to understand the safety profile of medicine and the benefit-risk balance. Pharmacoeconomics and the social impact of healthcare on patients and public health are also featured. It is written in a clear and straightforward manner to enable rapid review and assimilation of complex information and contains reader-friendly features.As a greater understanding of these aspects is critical for students in the areas of pharmaceutical medicine, clinical research, pharmacology and pharmacy, as well as professionals working in the pharmaceutical industry, this book is an ideal resource. Includes detailed coverage of current trends and key topics in pharmaceutical medicine, including biosimilars, biobetters, super generics, and Provides a comprehensive look at current and important aspects of the science and regulation of drug and biologics discovery
Author: Jonathan Herring
Publisher: Oxford University Press, USA
ISBN: 0198702264
Category : Law
Languages : en
Pages : 699
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Book Description
"A concise text providing discussion of the law and an overview of the ethical perspectives, ensuring that readers are able to fully understand the law and its context. Jonathan Herring's lively and captivating writing style brings this highly topical aspect of law to life, whilst remaining closely tailored to course requirements ensuring that this book is the perfect study companion. Carefully created features throughout the text draw attention to the many diverging opinions in medical law, including: religious, feminist, and European perspectives to ensure that readers develop a fully rounded appreciation of the complexities of the subject. As the most regularly updated medical law text, you can be confident that the book takes account of the most recent developments in this extremely fast moving subject area."--Publisher's website
