Risk-Based Monitoring: The Data Management Connection

Oct 6, 2018, 18:21 PM
Course ID : 122
Acronym : CSMN
Secure data quality in our Risk-Based Monitoring course. Discover the power of CDM and proactively address data aberrations. Enroll today!

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.

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

Registration Fees

$735

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 +1 781.972.5400 or toll-free in the U.S. 800.856.2556 for pricing.

Note: Due to COVID-19, we understand that most teams cannot currently dial-in together. As such, we are able to offer additional logins at a highly reduced rate. Please contact Barnett Customer Service at +1 781.972.5400 or toll-free in the U.S. 800.856.2556 to register with your additional participants requiring login credentials. Or email Customer Service at: customer.service@barnettinternational.com

Accreditation Information

Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education.  Participants will receive 2 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 issue a receipt of completion for earned CEUs within three weeks of program completion.  ACPE#: 0778-0000-22-009-L04-P. Released: 5/22. 

Hold this course at your company! For more information, contact Naila Ganatra at +1 215.413.2471. 

Series :
  • Clinical Trials & Translational Medicine
Topics :
  • Clinical Research
Job Functions :
  • Clinical Operations & Trial Management
  • Clinical Quality Assurance
  • Clinical Research Associate
  • Clinical Research Coordinator
  • Clinical Research Investigator
  • Data Management
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