Clinical services

We support you throughout the development of your clinical trials


AdHoc's experienced physicians and clinical research professionals assist you in the planning, of clinical trials.

We can help you in building the best  protocols by advising on study endpoints, eligibility criteria, study assessment and design options, and writing protocol synopses.

Protocols are designed to address timely recruitment of patients, and a provision of sound answers to scientific questions. You will receive excellent clinical study oversight which is paramount for a successful, timely, and cost-efficient drug development process.


Ah Hoc clinical team can support you with the following services:

  • Study Design
  • Eligibility criteria analysis
  • Endpoints definitions
  • Protocol development
  • Assessment of study competitive environment
  • Clinical centres selection
  • Investigator qualification
  • Assessment of patient recruitment strategy
Medical data review
Safety signal identification and safety review
Clinical Study Report preparation

Our experience extends across all major therapeutic areas, including:

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