Skyscape Web Viewer : Pharmacy Practice and the Law : Main Index

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Certificate of Registration application for revocation of - Daniel Family Pharmacy
certification requirements, electronic transmission prescriptions
See current good manufacturing practices (CGMP) Adulteration Cosmetics Current Good Manufacturing Practice Defining and Distinguishing Drugs from Foods, Dietary Supplements, Devices, and Cosmetics Dietary Supplements vs Drugs Drug Quality and Security Act of 2013 Drug Quality and Security Act of 2013 FDAMA's Compounding Provisions (§ 503A): Later Reinstated as § 503A Under the DQSA Medical Devices Pharmacy Compounding vs Manufacturing See current good manufacturing practices (CGMP)
change being effected (CBE) supplement The Road to an Approved New Drug Application Whether FDA-Approved Labeling Preempts State Product Liability Actions
Omnibus Budget Reconciliation Act of 1990 (OBRA ‘90) drug utilization review (DUR) off-label uses of medications overview standards of practice State Regulation of Third-Party Plans The Omnibus Budget Reconciliation Act of 1990
online pharmacies
opiate dependence
opinion, defined
opioid products addiction treatment programs prescriptions validity
opioid treatment programs (OTPs) methadone Opioid Treatment Programs Purpose of a Controlled Substance Prescription treatment of addicts
oral prescriptions, dispensing of
Orange Book
ordinances, overview
Oregon Board of Pharmacy
Orphan Drug Act (1983)
orphan drugs Reasons to Regulate Medicinal Drugs The Patient Safety and Quality Improvement Act of 2005
orthotics
See over-the-counter (OTC) drugs Federal Regulation of Medications: Development, Production, and Marketing See over-the-counter (OTC) drugs Use and Disclosure of PHI; Right to Access
chart orders
Chemical Diversion and Trafficking Act (1988)
child-resistant containers
Cholestin
citizenship requirements, licensing
civil court procedures
civil law, overview
Civil Rights Act of 1964
claims Dietary Supplement Health and Education Act 1994 false advertising False Claims Act food health claims health/disease
classification system Schedule I (Drugs and Other Substances) schedule I drugs schedule II drugs schedule III drugs schedule IV drugs schedule V drugs
clinical judgment exercises
clinical trials application for registration informed consent investigational drugs, access to Investigational New Drug (IND) application registration requirements