Clinical Trial Regulations With ICH GCP E6 R2 Workshop

The Clinical Trial Regulations With ICH GCP E6 R2 Workshop covers topics such as:

  • EU Annex 13
  • GCP requirements for the sponsor related to IMP
  • Distribution to sites
  • Handling of IMP at sites
  • Handling of IMP temperature deviations and complaints
  • Transfer of IMP between sites

The Clinical Trial Regulations With ICH GCP E6 R2 Workshop brings together:

  • Biotech companies
  • Clinical Research Organizations
  • Large to small Pharmaceutical companies
  • Clinical Research Services Suppliers
  • Non-Commercial Research Organizations

Future Events

Clinical Trial Regulations With ICH GCP E6 R2 Workshop 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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