Begin a career in the rapidly expanding clinical research industry. In this eighth session of the series, we will delve into regulations and guidelines followed in clinical research and introduce Good Clinical Practice.
Upon completion of this course, you will be able to: describe the purpose of the Code of Federal Regulations, ICH Guidelines, and HIPAA/Privacy Rule in the context of clinical trails; and describe differences in regulations for devices, orphan drugs, and expanded access programs, compared to routine clinical trials.
Attend only the sessions that interest you most, or register for all 12 sessions for the price of 10. Attend 10 sessions to receive a Professional Certificate of Completion in Clinical Research Foundations.