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State and Federal Pharmacy Law Study Guide - Florida

Contents: (287 pages including 90 practice exam questions and answers) Florida State Statutes and Florida State Administrative Rules. Federal Drug Control Law and Federal Controlled Substances Law.
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$99.95

State and Federal Pharmacy Law Study Guide - Texas

Contents: (243 pages including 60 practice exam questions and answers) Texas State Statutes and Texas State Administrative Rules. Federal Drug Control Law and Federal Controlled Substances Law.
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$99.95

Pharmacist Legal Responsibilities under Federal Law

Pharmacist Legal Responsibilities Under Federal Law. Covers: Introduction to Government and Law, FDA, Federal Drug Control Law, DEA, Federal Controlled Substances Law, Professional Liability and Risk Management, and selected Pharmacy Court Cases.
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$69.95

Florida Chapter 456 "Health Professions and Occupations"

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$19.95

Florida Chapter 465 "Florida Pharmacy Act"

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$19.95

Drug Enforcement Administration Narcotic Treatment Program Manual

Official guidance from the DEA on the steps to take in establishing and managing a narcotic treatment program under federal law.
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$19.95

Pharmacy Errors: A Course in Quality-Related Events (8hr – Approved For Florida Board of Pharmacy “Misfill” Discipline)

This program is designed to educate readers on the basic elements of human error and how they apply to the practice of pharmacy. Theories of human error are discussed, followed by a discussion of factors that can influence error capture, production and prevention and error analysis techniques like Root Cause Analysis (RCA). Finally, the course concludes with a summary of main ideas in order to become more “error-aware.”
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$279.00

The Newly Approved Drug

A new drug has recently been approved by the FDA. Two drugs within the same class have been withdrawn from the market due to safety issues, while one other drug in the class remains on the market. What should you do?
Immediately place the drug in stock.
Wait 6 months to stock the drug, to make sure it has no serious unknown risks.
Verbally counsel patients about the unknown risks of the new drug.
Require written informed consent of patients for the first 6 months.
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