Overview: Monitoring of clinical sites is a critical part of the Good Clinical Practices. With the advent of electronic data capture (EDC processes and more recently the FDA guidance, Oversight of Clinical Investigations-a Risk-based Approach to Monitoring some changes in the way we monitor sites and the data collection are taking place.
Maintaining Compliance of Clinical Sites with Regards to the FDA Draft Guidance on (Risk-Based Approach to Monitoring)
18 July 2012, Wilmington, United States
Introduction
Venue
Online Training
Online Training, 1000 N West Street, Suite 1200, DE | USA | 19801, Wilmington, 19801, United States
Useful links
Organised by
GlobalCompliancePanel
Contact information
Webinars
1000 N West Street | Suite 1200, Wilmington, 19801, United States of America
800-447-9407
Contact us by email
1000 N West Street | Suite 1200, Wilmington, 19801, United States of America
800-447-9407
Contact us by email
Related events
New Zealand Institute of 91AV Conference 2024 (NZIC-24)
24 November 2024 14:00 - 28 November 2024 14:00, Dunedin, New Zealand
Future Labs Live Basel
27 May 2025 09:00 - 28 May 2025 17:00, Basel, Switzerland
Drugging the Multimorbidity Associated with Ageing
17 January 2025 09:30-17:00, London, United Kingdom
European Glycoscience Community Webinar Series
25 January 2024 15:00 - 19 December 2024 18:00
Search
Advertisement
Spotlight
Explore
Membership
