Baltic Clinical Sites
Clinical trial sites · Latvia

Sites that enrol above the median. Run as one network.

Experienced investigators in rheumatology and primary care near Riga, plus specialists brought in for your indication. One feasibility answer, one budget and contract for all sites, agreed in 2–4 weeks.

Quick feasibility

Will we recruit your study?

Pick the indication and how many patients you need. You see our past enrolment against the median site straight away.

Indication
Phase
Patients needed from Latvia
Track record

Enrolment against the median site

Patients enrolled at our lead site and at the median site in the same trial. 16 industry trials with complete data, 2012–2025.

Our siteMedian site in the same trial

Sponsors we have worked with: .

Study list

Industry trials at our sites

All trials are public on ClinicalTrials.gov. Filter by area; click a registry number to open the record.

StartSponsorIndicationPhaseOur roleStatusRegistry
Therapeutic areas

Where we recruit best

Enrolment rates are patients per site per month, ours against the median site.

Network

Five sites within 40 km of Riga

One coordinator can cover several sites in a day, and monitors can combine visits. For specialist studies, visits can also run in the investigator's own office in Riga.

Schematic, not to scale.
IDSiteLocationRole
Investigators

Who runs your study

Each study has a principal investigator and a sub-investigator, several coordinators and study nurses as needed. Full CVs and GCP certificates come with the feasibility package.

What the network does

The work that slows sites down, done centrally

Feasibility

One answer for all sites, with patient pools, staff and equipment.

Start-up and contracts

One budget and one contract template for all sites, agreed in 2–4 weeks. Ethics and State Agency of Medicines documents.

Patient pre-screening

Practice records reviewed for eligible and newly diagnosed patients, GDPR-compliant.

Staff for your other sites

Our experienced coordinators and sub-investigators can also support other Latvian sites in your study.

Data and quality

Timely eCRF entry, fast query resolution, a quality check before every monitoring visit.

Specialists on demand

We bring in the specialist your protocol needs and train them on GCP and the protocol before first patient in.

Contact

Send a synopsis. Get one answer for all sites.

Confidentiality agreements are signed centrally for all sites.