Issue Detection and Escalation in Clinical Trial Settings 2012
10 Apr 2012
Webinar
Key Topics
Preventive risk mitigation methods including training and monitoring sites
Checking the investigators and IRB qualifications and training
Issuing protocol deviations
Considerations for protocol violations
Monitor report templates
Communication plans with issue escalations and contingency planning
Process maps for risk mitigations and action items including escalation
Who should Attend
Project managers, Clinical operations, Clinical Trial Associates (CTA), Clinical Research Associates (CRA), Pharmacovigilance specialists, Medical monitors, Principle Investigators and Site managers.
Past Events
Issue Detection and Escalation in Clinical Trial Settings 2012 - 10 Apr 2012, Webinar (26432)
Issue Detection and Escalation in Clinical Trial Settings 2026
Important
Please, check "Issue Detection and Escalation in Clinical Trial Settings" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Medical device, Medical laboratories, Pharma
