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Course Description

Clinical trials are critical to demonstrate drug safety and efficacy. This course will examine the process of conducting clinical trials, including considerations for recruitment of patients, drafting of research protocols and informed consent forms, regulatory considerations, financial disclosure, and investigator recruitment. This course will also examine stakeholder roles and responsibilities including that of institutional review boards, investigators and regulatory bodies, including a discussion of specific case studies and examination of primary scientific data.

Requisites

Prerequisite: CHY 142

Relevant Programs

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Thank you for your interest in this course. It is not scheduled for the current academic year.

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