Fundamentals of Clinical Trials (English)
Clinical trials are designed to answer questions concerning the safety and effectiveness of medical products. Get an overview of clinical trials regulated by the FDA. Learn about the planning process underlying the Strategic Clinical Plan and regulatory submissions to the FDA. Explore topics including protocol development and implementation, i.e. study site selection, financial controls, timelines, and management of the site's operations; proper informed consent; Good Clinical Practices compliance; HIPAA; FDA regulations and guidelines; and post-market support studies.
Health Sciences Sch. | University of California, Irvine
Keywords: clinical trials,health science,medical products,US Food and Drug Administration,Strategic Clinical Plan,protocol development,proper informed consent,HIPAA
- Nancy Ann Schwartz
This work is licensed under a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 United States License.