Data Monitoring Committees (DMCs) effect on subject safety in clinical research and how to set it up to be effective
12 Oct 2010
Webinar
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
Past Events
Data Monitoring Committees (DMCs) effect on subject safety in clinical research and how to set it up to be effective - 12 Oct 2010, Webinar (8655)
Data Monitoring Committees (DMCs) effect on subject safety in clinical research and how to set it up to be effective 2026
Important
Please, check "Data Monitoring Committees (DMCs) effect on subject safety in clinical research and how to set it up to be effective" official website for possible changes, before making any traveling arrangements
