The law and regulation of medicines

Cover of: The law and regulation of medicines |

Published by Oxford University Press in Oxford, New York .

Written in English

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Subjects:

  • Drugs -- Law and legislation -- Great Britain

Edition Notes

Includes bibliographical references and index.

Book details

Statementedited by Peter Feldschreiber.
ContributionsFeldschreiber, Peter.
Classifications
LC ClassificationsKD3460 .L895 2008
The Physical Object
Paginationlii, 473 p. ;
Number of Pages473
ID Numbers
Open LibraryOL22653645M
ISBN 100199534675
ISBN 109780199534678
LC Control Number2008277691

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It is a reference work and source of expertise for legal, medical, and pharmaceutical professionals working in the fields of medicine regulation, medical law and product liability. "The Laws OF Medicine" by Siddhartha Mukherjee (acclaimed author of "The Emperor of all Maladeries" and "The Gene") is a short, engrossing, intellectually stimulating discussion that focuses on "medicine" as an uncertain science that despite all the technological advances still needs to rely on a one on one, doctor-patient, relationship to Cited by: 4.

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[Emily Jackson] -- The story of a medicine's journey through the regulatory system in the UK, from the definition of a medicine, through clinical trials, licensing, pharmacovigilance, litigation, marketing and funding. About Law and the Regulation of Medicines The principal purpose of this book is to tell the story of a medicine's journey through the regulatory system in the UK, from defining what counts as a medicine, through clinical trials, licensing, pharmacovigilance, marketing and funding.

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Weissman has also authored the book “A Guide to California Community Pharmacy Law” and discussed the importance of laws that are aimed to curb prescription drug abuse. Controlled substance prescriptions must be issued for a legitimate medical purpose by a : Jennifer Gershman, PharmD, CPh.

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Laws Governing the Qualifications / Practice and Conduct of Professionals. Law Governing Storage / Sale of Drugs and Safe Medication. Law Governing Biomedical Research. Law Governing to Management of Patients. Law Governing Medico Legal Aspects. Law Governing The Safety of Patients, Public and Staff within the Hospital Premises and.

Regulations help to ensure quality drug products. FDA monitors drug manufacturers' compliance with Current Good Manufacturing Practice (CGMP) regulations. Siddhartha Mukherjee Author Biography.

Siddhartha Mukherjee is the author of The Emperor of All Maladies: A Biography of Cancer and The Gene: An Intimate History, winner of the Pulitzer Prize in general nonfiction, and The Laws of is the editor of Best Science Writing Mukherjee is an assistant professor of medicine at Columbia University and a cancer physician and.

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guidelines, recommendations. law and ethics in medical practice overlap in many areas and yet each has its unique parameters and distinct focus. Legal and Ethical Regulations of Medical Practice in History In ancient Egypt, practice of medicine was subject to legal restrictions.

The right to practise was restricted to members of a certain class, and all doctors had to learnFile Size: 37KB. Drug Regulation: History, Present and Future 67 take informed decisions about all aspects of medi-cines without special training and access to nec-essary information.

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The regulation of therapeutic goods, defined as drugs and therapeutic devices, varies by jurisdiction. In some countries, such as the United States, they are regulated at the national level by a single agency. In other jurisdictions they are regulated at the state level, or at both state and national levels by various bodies, as in Australia.

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effective regulation of medicines across the EU. Different authorisation routes: one set of common rules. EMA enables one application, one assessment, one market authorisation for the whole of the EU.

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