Risk Based Monitoring for GCP Compliance 2019

  • 27 Mar 2019
  • Webinar

Description

Risk Based Monitoring for GCP Compliance 2019 is a webinar that covers topics such as:

  • Understand risk based monitoring tools and methodology used in clinical research projects
  • Define risk based monitoring for clinical trials
  • How to plan risk based monitoring approaches for clinical trials
  • Explore the roles and responsibilities of those involved in risk based monitoring
  • Develop and apply risk monitoring in your clinical trials
  • Understand how to identify and evaluate study site and protocol risks for targeted SDV
  • Learn how to document risk based monitoring in the monitoring plan

Risk Based Monitoring for GCP Compliance 2019 is intended for:

  • Clinical operations personnel
  • Clinical development managers and personnel
  • Clinical research archiving and document management personnel
  • Clinical research associates
  • CROs using laboratories to analyze clinical trial samples
  • Quality assurance managers and auditors
  • Sponsors and non-commercial sponsors
  • Project management
  • Laboratories analyzing samples from clinical trials
  • Consultants
  • Legal and regulatory authorities
  • Regulatory affairs personnel

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Important

Please, check "Risk Based Monitoring for GCP Compliance" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Legal, Management, Operations, Quality assurance

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