ICH GCP – Establishing and Following Good Clinical Practice

ICH GCP – Establishing and Following Good Clinical Practice


This webinar’s goal is to create awareness and provide advice on the practical issues of Good Clinical Practice as well as to get a better understanding of the regulatory requirements and to raise awareness on possible problem areas.  Former FDA Investigator Christopher Rush conducted over thirty (30) BioMedical Monitoring (BIMO) Inspections while employed by the FDA and has worked for a large pharmaceutical manufacturer as  a Clinical Quality Assurance Auditor.  Currently, Chris is a consulting to pharmaceutical companies worldwide offering Clinical QA advice and performing on-site audits of Investigator Sites, Sponsors and CROs.  Chris will discuss the ideals behind ICH GCP, how to implement them at a Sponsor and Site level and offer real world examples of good and bad Good Clinical Practices.

Who should attend:

  • Clinical Affair Professionals
  • Executive Management
  • Quality Assurance Professionals
  • Regulatory Affair Professionals
  • Risk Management Professionals
  • Subject Matter Experts
  • All personnel wants to learn about Good Clinical Practice

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