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 and one point of contact. The same budget and contract template for every site, negotiated by us in 2–4 weeks.
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.
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.
Sponsors we have worked with: .
Industry trials at the lead site (M & M centrs)
All trials are public on ClinicalTrials.gov. Filter by area; click a registry number to open the record.
| Start | Sponsor | Indication | Phase | Our role | Status | Registry |
|---|
Where we recruit best
Enrolment rates are patients per site per month, ours against the median site.
Fifteen sites in Latvia, Lithuania and Estonia
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.
| Site and therapeutic areas | Location | Type |
|---|
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.
The work that slows sites down, done centrally
Feasibility
One answer for all sites, with patient pools, staff and equipment.
Start-up and contracts
The same budget and contract template for every site; we negotiate each site agreement, typically 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.
Join the network as an investigator
No research experience needed. We train you on GCP and the protocol, handle contracts and budgets, and send coordinators.
- Industry-paid studies in your own practice or office
- Your patients get access to new treatments
- We do the paperwork, coordination and data entry
- Same budget and contract template for every site, agreed in 2–4 weeks
Send a synopsis. Get one answer for all sites.
Confidentiality agreements are signed centrally for all sites.