Begin a career in the rapidly expanding clinical research industry. In this tenth session of the series, we will explore the importance of good documentation practices and essential documents.
Upon completion of this course, you will be able to: describe the purpose and importance of essential documents from regulatory, data quality, and human subjects' protection perspectives; and, discuss the role of various personnel at the sponsor/CRO and sites regarding essential documents.
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.