Challenges and opportunities in implementing the new guidance
New requirements of the updated ICH GCP guideline
Best practice of additional new GCP requirements which will facilitate a broad and consistent international implementation of new methodologies for running clinical trials
New requirements for Sponsor Oversight, CROs, quality systems, risk based approaches and the TMF
Who should Attend
Professionals working in:
Regulatory affairs and pharmacoviglance in pharmaceutical
Clinical research/clinical operations
CRO
Biotechnology
Clinical trial supply
Regulatory authorities and study sites
Document management
Quality assurance
Legal
Past Events
The New ICH GCP E6 R2 Guideline 2019 - Feb 2019, The Rembrandt Hotel, London, United Kingdom (73685)
The New ICH GCP E6 R2 Guideline 2018 - 25 Sep 2018, The Rembrandt Hotel, London, United Kingdom (68401)
The New ICH GCP E6 R2 Guideline 2018 - 27 Feb 2018, The Rembrandt Hotel, London, United Kingdom (68399)
The New ICH GCP E6 R2 Guideline 2017 - 22 Sep 2017, The Rembrandt Hotel, London, United Kingdom (68400)
Important
Please, check "The New ICH GCP E6 R2 Guideline" official website for possible changes, before making any traveling arrangements
Event Categories
Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Medical laboratories, Pharma
