ComplianceOnline Webinar - Data Monitoring Committees (DMCs) effect on subject safety in clinical research and how to set it up to be effective(October 12, Tuesday 10:00 AM PDT | 01:00 PM EDT)

This Data Monitoring Committees (DMC) webinar will guide you through the essential and the purpose of the Data and Safety monitoring plan.
Areas Covered in the Seminar:

  • The historical background of why Data and Safety monitoring is essential.
  • The purpose of the Data and Safety monitoring plan.
  • The Regulatory requirements for safety monitoring.
  • Studies requiring a formal Safety Monitoring Committees.
  • What does the "Charter" of a DMC compose of?
  • What is the composition and function of a DMC?
  • What types of studies "require" a DMC?
  • Conflict of interest and the DMC.

Who Will Benefit:
This Webinar will provide invaluable assistance to the pharmaceutical industry and to investigators and their staff in the regulatory / legal responsibilities and also the ethical considerations in pharmaceutical product (Drug or device) research involving human subjects. Those benefiting the most would be:

  • Principal Investigators / Sub-investigators.
  • Clinical Research Scientists (PKs, Biostatisticians,)
  • Safety Nurses
  • Clinical Research Associates (CRAs) and Coordinators (CRCs)
  • Recruiting staff
  • QA / QC auditors and staff.
  • Clinical Research Data managers

For More Information: