Back To News
Add these series to your organization’s subscription
Learn more about Summit Clinical Research courses
New Summit Clinical Research Courses
Four new Summit courses provide a comprehensive overview of key aspects of clinical research, from Quality Control (QC) reviews to participant retention strategies. Learners will explore QC’s role in documenting informed consent, eligibility criteria, adverse events, and protocol deviations, along with the use of Corrective and Preventative Action (CAPA) plans. They will also learn the essential functions that Good Documentation Practices (GDP) play in creating and maintaining study documents. Additional topics include laboratory requirements, kit management, biohazard safety, and communication between labs and clinics. Lastly, discussions on participant retention and compliance strategies emphasize the importance of respect, communication, and effective management of study dropouts.
New courses:
- Summit: Quality Control
- Summit: Study Documents
- Summit: Clinical Research Laboratory
- Summit: Participant Retention
Audience
Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), Contract Research Organizations (CROs), Faculty, Institutional Officers, Investigators, Laboratory Personnel, Quality Control/Quality Management Professionals, Regulatory Affairs Professionals, Research Administrators, Research Assistants, Sponsors, Study Sites
