You can delegate anything from study start-up to site close-out to us. Whether you require a single service or want to entrust us with a complex project, we are ready to hit the ground running!

 

 
 

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FIELDS OF EXPERTISE

  • Drugs (Phase I-IV trials, PASS/PAES studies, Managed Access Programs, ATMPs)
  • Devices (pre- and post-CE label)
  • IVDs (performance evaluations)
  • Non-interventional studies

APPROACH

  • We combine high level international experience with local know-how and experience
  • We provide personalised guidance and assistance in all stages of your research
  • We have a complete set of ICH-GCP proof SOPs to assure quality and efficiency of all services delivered

KEY ADVANTAGES

  • Work is done according to Ad Hoc Clinical's SOP's permitting fixed fees
  • Management and quality control is done by Ad Hoc Clinical
  • You maintain oversight without having to manage day-to-day activities