The New ICH GCP E6 R2 Guideline

The New ICH GCP E6 R2 Guideline is a conference that covers topics such as:

  • 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

The New ICH GCP E6 R2 Guideline brings together 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

Future Events

The New ICH GCP E6 R2 Guideline 2020

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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