During monitoring visits, one of the most important and impacting activities that a Clinical Research Associate (CRA) performs is the source document verification of Adverse Events (AEs). The CRA serves as the eyes for the research sponsor when it comes to proper collection and documentation of subject safety information. Incorrect and inadequate monitoring of AEs can lead to inaccurate labeling for clinical trials and impact market application inspectional reviews, as well as post marketing labeling. The safety, regulatory, and ICH definitions will be reviewed and applied to the monitoring process in this web seminar. This includes Causality, Expectedness/Unanticipated, and other important concepts. Case scenarios will be used to apply the information for better learning.
- Define safety concepts and reporting requirements
- Recognize the importance of verifying the subject baseline history
- Determine when to start and stop monitoring AEs
- Apply a detailed presentation of the source document verification process of AEs
- Manage challenges in monitoring AEs
- Verify appropriate credentialing for site AE evaluation of event relationship
- Appreciate the impact of monitoring on future product labeling
- Discuss reporting trends
- Device and Drug Study Clinical Research Associates
- Contract Clinical Research Associates
- Clinical Research Associate Managers
- Project Managers
Jackie Stader, C.O.T., C.C.R.C.
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Includes up to 20 participants at one site. All participants (up to 20) are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met. For groups larger than 20 or for additional sites, please call 1-800-856-2556 for pricing.
Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. Participants will receive 2.0 hours (0.2 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation. Barnett International will mail ACPE statements within three weeks of program completion. ACPE#: 0778-0000-14-016-L01-P. Released: 5/14.
Hold this course at your company! For more information, contact Naila Ganatra at (215) 413-2471.