We're still actively developing this site. If you encounter any issues, please report them! - Report an issue

LEGAL STRUCTURES FOR CONTROLLED SUBSTANCES

PHARMACY 612
Course Description

Discusses federal statutes and regulations related to drug manufacturing, drug distribution, and drug use, with an emphasis on drug scheduling and controlled substances. Describes the governmental framework within which pharmaceutical development is regulated and practiced. Covers statues and regulations protecting human subjects' privacy and autonomy in research.

Prerequisties

Declared in MS Pharmaceutical Sciences: Psychoactive Pharmaceutical Investigation or Capstone Certificate in Psychoactive Pharmaceutical Investigation

Satisfies

This course does not satisfy any prerequisites.

Credits

1

Offered

Not Applicable

Grade Point Average
3.65

1.09% from Historical

Completion Rate
97.62%

1.52% from Historical

A Rate
54.76%

-15.42% from Historical

Class Size
42

-19.23% from Historical

Instructors (2025 Fall)

Sorted by ratings from Rate My Professors

Similar Courses

DRUG HISTORY: DANGEROUS DRUGS AND MAGIC BULLETS

PHARMACY 563

A history of medicinal substances and dangerous drugs in wider context, with a focus on gender, race, class, business, and other analytical categories. "Medicines" and "drugs" change over time -- and concepts of risk, danger, legality, and even scientific evidence are elastic. Histories of laws, regulations, and key historical actors, as well as specific drug biographies, will be provided.

PHARMACY LAW AND REGULATION

S&APHM 611

Federal and Wisconsin laws related to drug manufacture, drug distribution, drug use, and pharmacy practice.

GRADUATE SEMINAR IN HEALTH-SYSTEM PHARMACY

PHMPRAC 962

Specialized subject matter of current interest to graduate students in the MS Pharmacy Administration program.

SELECTED TOPICS IN PHARMACY

PHARMACY 490

Various topics related to the Pharmacy profession.

INTRODUCTION TO REGULATORY PRACTICE

PHMSCI 751

Identifies and examines the key regulatory agencies and practices that govern the highly regulated and diverse pharmaceutical industry. Highlights current and emerging FDA and ICH regulations and guidance documents to successfully navigate meeting with the agencies and to submit required documentation for successful product development.