Clinical research across Eastern Europe
Clinical Trials in Ukraine
Experienced regional support with study planning adapted to current regulatory, operational and safety conditions.
Discuss your study
Clinical research support in Ukraine
- Experienced clinical research professionals and investigators.
- Recruitment potential across several therapeutic areas.
- Study delivery must be assessed against current regulatory, infrastructure and safety conditions.
- Risk-based planning and sponsor alignment are essential before activation and throughout delivery.
Regulatory and ethics framework in Ukraine
Ukraine is not part of the EU CTIS system, so studies follow national procedures involving the Ministry of Health, the State Expert Center and local ethics committees. Current conditions can affect timelines and operations, so we confirm requirements and risk arrangements for each study at the start.
Typical start-up workstreams in Ukraine
- Country feasibility: review of the protocol against local standard of care, investigator interest and patient availability.
- Regulatory and ethics submissions: preparation, translation and tracking of submission packages and responses to authority questions.
- Contracts and budgets: site agreements, budget negotiation and insurance documentation.
- Site activation: qualification, training, essential documents and investigational product logistics.
- Conduct and oversight: monitoring, issue escalation and sponsor reporting through close-out.
Timelines, authority requirements and site capacity change over time, so we confirm current conditions for your protocol during feasibility rather than quoting generic figures.
Multi-country studies
Many sponsors combine Ukraine with neighbouring countries to reach enrolment targets.