Why choose us

  • Expertise BioVirtus can execute large long-confinement studies with up to 45 subjects.
  • Effectiveness Thanks to a large database of subjects BioVirtus guarantees swift and effective recruitment, screening and enrolment.
  • Easiness We have the ability to quickly enrol patients with various diseases.     

Start-up Activities

At the initiation stage of the clinical study BioVirtus offers the following services:

  • scientific and business consulting of clinical study assumptions
  • feasibility study based on the protocol outline, study timelines as well as the IRB/IEC
    and regulatory requirements
  • medical writing or review of the study documentation: Protocol, Informed Consent Form,
    Case Report Form, Clinical Trial Application, etc.
  • submission of clinical study documentation and day-to-day contact with IEC/IRB and Regulatory Authorities
  • preparation of detailed study budget, negotiations and sub-contracting (e.g. PK laboratories)
  • study-specific trainings for clinical research team (investigators, nurses, laboratory technicians, pharmacist, coordinators)
  • scientific contacts with certified pharmacokinetic and analytical laboratories
  • preparation of study-specific operational documentation (medical history, logs, etc.).