FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program - Webinar By GCP 2011
10 May 2011
Webinar
The webinar deals with FDA perspective for Auditing or Inspecting a study, The Sponsor`s responsibility and monitoring system components, Protocol knowledge, preventing errors, Preparation for an audit or inspection and Measures for quality monitoring.
The event brings together personnel from Pharmaceutical, Biotechnology and CRO industries.
Past Events
FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program - Webinar By GCP 2011 - 10 May 2011, Webinar (15148)
FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program - Webinar By GCP 2026
Important
Please, check "FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program - Webinar By GCP" official website for possible changes, before making any traveling arrangements
Event Categories
Government & Global Issues: Law & Regulations
Health & Medicine: Hospitals & Clinics, Medical device, Medical laboratories, Pharma
