The Drugs and Cosmetics Act of India

The Drugs and Cosmetics Act of India

An Act to regulate the import, manufacture, distribution and sale of drugs 2[and cosmetics]; WHEREAS it is expedient to regulate the 3[import, manufacture, distribution and sale] of drugs 2[and cosmetics];

AND WHEREAS the Legislature of all the Provinces have passed resolutions in terms of section 103 of the Government of India Act, 1935 (26 Geo. 5, c.2), in relation to such of the above-mentioned matters and matters ancillary thereto as are enumerated in List II of the Seventh Schedule to the said Act.


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Dale and Appelbes Pharmacy Law and Ethics, 9th Edition

Dale and Appelbes Pharmacy Law and Ethics, 9th Edition
Pharmaceutical Press | 2009 | ISBN: 0853698279 | 553 pages | PDF | 1,9 MB

This is a comprehensive guide to law and ethics for pharmacy practice in the UK. “Dale and Appelbe’s Pharmacy Law and Ethics” has become established as the standard student textbook and reference work on this subject in the UK. A knowledge of pharmacy law is a substantial and compulsory component of the undergraduate and pre-registration pharmacy syllabus in the UK and changes to the syllabus and practice require the text to be updated regularly. This revised edition provides a comprehensive guide to the law that affects the practice of pharmacy and the use of medicines in Great Britain, and complete coverage of the pharmacy undergraduate and pre-registration syllabus and British law relating to medicines and poisons.
Gordon E. Appelbe, Joy Wingfield, “Dale and Appelbe’s Pharmacy Law and Ethics, 9th Edition”


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Pharmacy Law and Practice

Pharmacy Law and Practice

This textbook explains what pharmacy students and practicing pharmacists need to know about pharmacy and the law, including recent changes in the National Health Service. The book provides easy accessibility amd concise, yet comprehensive information. There have been many changes in the NHS and in the law relating to pharmacy since the first edition was written. Therefore, the book has been thoroughly revised, and the text re-organized.

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Essentials of Pharmacy Law

Essentials of Pharmacy Law

This book examines the laws and regulations relating to the practice of pharmacy, and the regulation and control of drugs cosmetics, and medical devices. Most available pharmacy law texts thus far have been written by lawyers and present heavy, dense, legalistic reading that focuses on legal theory. Essentials of Pharmacy Law is written by a practicing pharmacist in clear, accessible, contemporary prose that concentrates on application. This user-friendly text is a compilation and commentary of selected federal laws and regulations pertaining to the general practice of pharmacy in the United States. It covers topics in a simple and concise format. Furthermore, case studies and review questions and a bulleted summary of key points make for easy reading and aid in comprehension. Essentials of Pharmacy Law will be extremely useful to senior pharmacy students preparing for the Multi-State Jurisprudence Exam (NABLEX MJPE). as well as the voluntary Pharmacist Competency Exam offered to practicing pharmacists. It alsoalso serves as a valuable reference for pharmacy students, practicing pharmacists seeking licensure by reciprocity and/or preparing for the MJPE, pharmacy technicians who are in need of a comprehensive update, and other interested healthcare professionals.

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Pharmacy Law: Textbook and Review

Pharmacy Law: Textbook & Review

A concise, two-in-one review of pharmacy law-ideal for coursework and MPJE® exam prep!
This accessible, real-world guide gets you ready for the practice of pharmacy, while giving you the proper training to be compliant with the law. To that end, the book expertly covers relevant laws, rules, and regulations, and it highlights the distinctions between state and federal law where appropriate. In no other reference can you find such a succinct, yet thorough review of the full range of federal pharmacy laws, including the Controlled Substances Act, the Food, Drug, and Cosmetics Act, the new Dietary Supplement Health Education Act, the FDA Modernization Act, and the Medicare Modernization Act.

Features:

•An excellent primer for coursework and unbeatable preparation for licensure and the MPJE®
•Opening chapter on drug regulation and standards provides you with a practical legal framework for subsequent chapter material
•Overview of the drug approval process and federal reporting programs
•Chapter on internet sales and FDA authority to act
•Coverage of opioid addiction treatment and narcotic treatment programs, giving you a unique close-up of the latest laws and policies
•Comprehensive set of 450 multiple-choice questions and answers
•Chapter of MPJE®-format practice questions

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Managing Relationships with Industry: A Physician's Compliance Manual

Managing Relationships with Industry: A Physician's Compliance Manual

Physicians in academic and private practice settings are increasingly engaged in collaborations and encounters with employees and contractors from the research and marketing arms of pharmaceutical and device companies. These activities are numerous and range from consulting and conducting research, to giving talks, meeting with sales representatives, to interfacing with industry on behalf of foundations and professional societies.

The primary aim of this book is to educate physicians about the rules, regulations, and guidlines relevant to and the potential pitfalls of collaborating with industry so that physicians may enter into allowable relationships with industry with the knowledge necessary to mitigate the possible legal risks.

* Will help physicians stay abreast of the new rules for continuing medical education (CME)
* Addresses the increasing amount of international commercial, academic and clinical collaboration
* Discusses the growing and accelerating regulatory environment that defines the scope and boundaries of physician-industry relationships

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