Demonstrative Documents in Clinical Research Compliance

Demonstrative Documents in Clinical Research Compliance is organized by Society of Clinical Research Associates (SOCRA).

Termination Date: 12/22/2026

Description:
A study’s protocol must be followed in order to maintain compliance. In order to demonstrate compliance, the study team should implement dynamic documentation that clearly and concisely tells a subject's story of participation in the clinical study. By prioritizing adherence to the protocol and documentation of the subject's experience, the study team will successfully demonstrate compliance and mitigate risk.

Learning Objectives:
At the completion of the webinar, participants should be able to:
• Discuss document creation and maintenance to support procedures described in the IRB-approved protocol.