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.
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.).