#Barnett
Purchase the recording of a web seminar you have attended in the past and SAVE 50%! Contact Barnett Customer Service for details: +1 781.972.5400 or toll-free in the U.S. at 800.856.2556.
Web Seminar Archives provided through Barnett’s Learning Management System (Single User access) or by electronic file transfer (Site License).
Site license archives are also available in SCORM format for LMS integration. Please contact Barnett at (215) 413-2471 for more details and pricing on SCORM files.
Bulk Archive access is available via Barnett’s Training Subscription. Click here to learn more.
Archive: Risk-Based Monitoring: The Data Management Connection
Course Description
The final guidance, “Guidance for Industry: Oversight of Clinical Investigations — A Risk-Based Approach to Monitoring” was released in August 2013. To quote from the new guidance, “…monitoring refers to the methods used by sponsors of investigational studies, or CROs delegated responsibilities for the conduct of IND studies, to oversee the conduct of and reporting of data from clinical investigations, including appropriate Clinical Investigator supervision of study site staff and third party contractors.”
We will examine the expectations for the clinical data management (CDM) contributions to assist in this initiative, and the role that CDM can play in ensuring that risk is minimized when it applies to data quality.
Video Preview
Learning Objectives
- Recognize the rationale regarding risk-based monitoring
- Illustrate the active role that CDM is expected to exhibit in this approach
- List the potential CDM reports to assist in identification of data aberrations
- Interpret the way forward for future CDM activities
Who Should Attend
- Clinical Data Managers
- Clinical Research Associates
- Clinical Trial Managers
- Project Managers
- Quality Assurance Personnel
Instructor
Denise G. Redkar-Brown, MT
Click here for complete trainer biographies
Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471.