Webinar on Focusing Investigational Sites Risks in RBM
MakroCare Organizing free online webinar on "Focusing Investigational Sites Risks in RBM". Investigational site risk assessment is essential for effective planning and implementation of clinical trial project. This webinar will give the insight of the steps in investigational oversight from risk identification, assessment steps and how to integrate them into site qualification and into the study.
- New York, NY (1888PressRelease) March 31, 2016 - Sponsor's performance of investigational site risk assessment is essential for effective planning and implementation of clinical trial project. Risk identification starts at the sponsor/CRO system and project level, and also risks are assessed and controlled at site level at pre-study and during the trial. The monitoring approach and content of the study monitoring plan must be based on this risk identification and assessment. This webinar will review site risk identification, assessment steps and how to integrate them into site qualification and into the study monitoring plan. This webinar will also focus on how to coordinate the sponsor quality systems to support risk-based approaches for monitoring and oversight.
Objectives:
Identify key investigational site risk categories per project and integration into site qualification and monitoring plan development
Recognize risk management factors to coordinate for investigational site oversight: risk assessment, tracking and controlling
Importance of centralized monitoring in monitoring investigational site risks
Role & responsibilities of central monitor in tracking and managing investigational site risks
Date/ Time: Tuesday, 5th April 2016 I 11 AM - 12 Noon EST
Speakers:
Sandra 'Sam' Sather, MS, BSN, CCRA, CCRC, Clinical Operations & Risk Expert
&
Ashok Ghone, PhD, VP, Global Services, MakroCare
Click here to register : http://www.makrocare.com/registration-from-for-live-webinar-focusing-investigational-sites-risks-in-rbm
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