Debra B. Feinberg – Pharmacy Law. Textbook and Review

Автор: Debra B. Feinberg
Название книги: Pharmacy Law. Textbook and Review
Формат: PDF
Жанр: Медицина, Управление и экономика фармации, право и закон
Страницы: 305
Качество: Изначально компьютерное, E-book

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:

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
Comprehensive set of 450+ MPJE(R)-format practice questions and answers

This is the first edition of Pharmacy Law: Textbook and Review. As an
Assistant Adjunct Professor at Albany College of Pharmacy in Albany,
New York for the past seven years, I have taught Jurisprudence to the fifth
year PharmD class. My primary goal in teaching Jurisprudence is to prepare
students for the Pharmacy Boards. The goal of this book is to prepare
you to be successful in your endeavor to pass the federal portion
of the Pharmacy Boards. For those of you who have been successful in
passing the Pharmacy Boards, this book will serve as a reference tool as
you advance the practice of pharmacy.
The book is divided into topics including a description of the federal
entities that guide and regulate the practice of pharmacy; a history of
pharmacy law; a demonstration of the drug approval process; a review
of drug product substitution; a comprehensive review of the controlled
substances act; a review of opioid treatment; an overview of medical
devices, dietary supplements, herbals, homeophathics, and cosmetics;
drug product packaging and labeling; and other regulations such as
HIPPA, USP 797, bar coding, and the methamphetamine act. Where possible
each chapter provides web sites helpful in further discussion of the
topic.