Investigator Initiated Trials - What Are We Doing to Ensure Human Subject Protection? 2013
06 Feb 2013
Webinar
Key Topics
Way to ensure human subject protections
The importance of investigator-initiated trials
What are the site responsibilities in investigator initiated trials
The investigator deficiencies
The resources available to help the investigator in the conduct of investigator-initiated trials
The approaches or concerns of Institutional Review boards
Who should Attend
Senior Clinical Research Associates(CRAs)
Principle Investigators
Contract Research Organizations (CROs)
Clinical Research Project Manager
Site Management Organizations (SMOs)
Institutional Review Boards (IRBs)
Past Events
Investigator Initiated Trials - What Are We Doing to Ensure Human Subject Protection? 2013 - 06 Feb 2013, Webinar (36537)
Investigator Initiated Trials - What Are We Doing to Ensure Human Subject Protection? 2026
Important
Please, check "Investigator Initiated Trials - What Are We Doing to Ensure Human Subject Protection?" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Medical device, Medical laboratories, Pharma
