by SOCRA | Jun 1, 2026 | Clinical Research Courses
Overview: This presentation will provide an overview of the sponsor responsibilities for conducting clinical research. The presentation will address sponsor responsibilities for regulatory submissions, site selection, documentation, and monitoring. Safety and...
by SOCRA | Jun 1, 2026 | Clinical Research Courses
Program Information: The FDA allows for charging for investigational products used in clinical research under certain circumstances. The federal regulations also state that participants should be informed of any additional costs that may result from participation in...
by SOCRA | Jun 1, 2026 | Clinical Research Courses
Updated December 2024: This learning module is intended to encourage the reader to maintain an understanding of current activities involved in the conduct of research involving human subjects. The module offers one SOCRA continuing education unit to those who complete...
by SOCRA | Jun 1, 2026 | Clinical Research Courses
Program Information: Ms. Rugloski will provide tips and examples for creating and implementing a Project Team Member Transition/Training strategy to ensure effective and efficient project team member transitions. The session will end with an activity comprised of an...
by SOCRA | Jun 1, 2026 | Clinical Research Courses
Overview: This online course will provide information on the purpose and components of a research protocol and helpful strategies for writing a protocol draft with an Institutional Review Board reviewer’s perspective in mind. Three steps to writing an abstract, the...
by SOCRA | Jun 1, 2026 | Clinical Research Courses
Program Information: 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...
