Clinical Trials


EuDRAcon’s network of companies can offer its expertise to support clinical research, for example, with the preparation and submission of the documentation in applications for Clinical Trial Authorisation.

  • Advice on the role of Voluntary Harmonisation Procedure (VHP)
  • Central and/or local ethics committee submission
  • Safety reporting
  • GCP audits

For more detailed information about our clinical trials services, please visit the individual websites of our group.