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Full Service

Our knowledge, experience and know-hows enable a full range of service for clinical studies phase II-IV as well as non-interventional studies for both medicinal products and medical devices. 

 

  • Consulting

  • Regulatory approval (BfArM, PEI, and local ethics committees)

  • ICH-GCP conformity
  • Auditing
  • Project management
  • Patient recruitment
  • Monitoring
  • Data management
  • Data analysis
  • Archiving
  • Pharmacovigilance
  • Medical writing
  • Publication
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