Strategic project support and consultancy

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Clinical trials are conducted to collect data regarding the safety and efficacy of new drug and device development. Communication throughout all phases of the clinical trial is essential to run successfully a clinical study and build successful and long-term partnership with pharmaceutical and biotech companies, CROs, research sites and patients.

We cover a broad spectrum of support activities and provide our clients with up to date country specific standards for regulatory activities, inner knowledge of submission in CEE countries. Our clinical development experts offer a range of services which includes:

  • feasibility studies protocol with investigator site selection
  • planning and coordination of investigator meetings
  • clinical operations such as site initiation, medical monitoring and study closeout
  • regulatory affairs and safety reporting
  • medical writing and translations
  • project management

Your project is safe in our hands!

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We work not to prove, but to improve!