Estonia, Latvia and Lithuania offer experienced sites, motivated participants and EU regulation in one compact region. Capture runs all three countries in one study, hosted in the EU, with site-level separation and one audit trail.
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Study region
Estonia, Latvia, Lithuania
Key points for studies in the Baltics
Research landscape
The Baltic states are small individually, but together they offer a population of around six million, university hospitals in Tallinn, Tartu, Riga, Vilnius and Kaunas, and investigators used to international trials. Sponsors often plan them as one region: a single CTIS application covering all three, a regional monitoring team, and sites activated in parallel.
The data system should reflect that. One study with site-level separation lets each hospital see only its own participants, while the regional team sees all three countries on one dashboard. Capture hosts the study in the EU (Frankfurt), so study data stays in the EU. See clinical trial software Latvia for the Latvian perspective in more detail.
Plan translations early. Consent forms and participant materials need approved versions in each language participants use, and validated questionnaires need official translations. Record which language version each participant received.
Randomised
96 / 120
Sites active
7
Open queries
12
Regional oversight
The study dashboard pulls enrolment, compliance, safety and site risk into one view, filtered globally, by country or by site. The site risk monitor rates each site red, amber or green and says why, so a regional monitor can see where to focus.

Add sites in each country in the free sandbox and compare them side by side.
Country by country
| Country | Medicines agency | Main research cities |
|---|---|---|
| Estonia | State Agency of Medicines (Ravimiamet) | Tallinn, Tartu |
| Latvia | State Agency of Medicines (Zāļu valsts aģentūra) | Riga |
| Lithuania | State Medicines Control Agency (VVKT) | Vilnius, Kaunas |
Ethics review arrangements differ by country. Check current national requirements for your study.
Recruitment
Specialist care in the Baltic states is concentrated in a few large hospitals, which often makes eligible patients easier to identify and helps recruitment in common conditions. For rare diseases, however, national patient pools are small, and targets should be set per country with that in mind.
Investigators and study teams commonly work in English with sponsors, while participant materials must be in the languages participants use. Plan monitoring visits across three countries as one regional route, and use the dashboard's country filter to compare enrolment and data quality between them. See multi-site clinical trial management.
Before you start
Covering each Baltic member state in the trial.
Ethics and national parts checked for each country.
Consent and participant materials in each language used.
Controller and processor roles, and data protection impact assessment.
Monitoring plan across three countries.
Ethics approval, contract, initiation visit and delegation log.
Investigators and study teams commonly work with sponsors in English, while participant materials must be in local languages.
They can be, but national patient pools are small, so set realistic targets per country.
Under the EU Clinical Trials Regulation, through CTIS, with national agencies and ethics committees in each country assessing their part.
Yes. A multinational application can cover all three, and Capture runs all sites in one study with site-level separation.
Often Estonian, Latvian, Lithuanian and sometimes Russian, depending on the participants.
Yes. Choose EU (Frankfurt) hosting at study setup.
Capture hosts study data in the EU (Frankfurt) or the US (N. Virginia), chosen at study setup, with AES-256 encryption at rest and TLS in transit. Choosing Frankfurt keeps study data in the EU.
Yes. The free sandbox has every feature with no credit card and no time limit.
Keep exploring
Clinical trial software Latvia
Latvia in detail.
EU CTR clinical trial software
The EU regulation.
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Data protection.
Clinical trial software for European universities
Academic sponsors.
Multi-site clinical trial management
Sites across countries.
Clinical trial software Germany
Another EU guide.
EU hosting, site separation, one audit trail. Free sandbox.