Clinical Trial Regulations With ICH GCP E6 R2 Workshop

  • 17-19 Sep 2019
  • Leonardo Hotel Amsterdam Rembrandtpark, Netherlands
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Description

Topics
  • 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
Who should Attend
  • Biotech companies
  • Clinical Research Organizations
  • Large to small Pharmaceutical companies
  • Clinical Research Services Suppliers
  • Non-Commercial Research Organizations

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Important

Please, check "Clinical Trial Regulations With ICH GCP E6 R2 Workshop" official website for possible changes, before making any traveling arrangements

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