Your clinical trial team in Finland and the Nordics
RecQ’s own CRAs start up, monitor and close out drug, device and IVD studies. One contact, one contract and a reply by the next working day.
- 150site visits in 2026
- 10countries
- 41submissions in 2026
- FDA, BfArM, Fimeahave inspected our studies
- ISO 14155certified
- CRA of the Year 2023Pharmaca
Figures for our internal team, status Q3 2026. See the details
We do the work ourselves
RecQ is led by Rekaut Naderipour, Pharmaca’s CRA of the Year 2023 and a GCP trainer who still monitors and manages studies himself. The CRAs you see on our About page are the ones who visit your sites.
People we know by name
Our own CRAs work as one team under one team lead, across the Nordics and in Germany, the Netherlands, Switzerland, Austria and Estonia. For other roles and regions we propose independent consultants we know personally.
You pay for hours worked
We invoice the hours actually worked, not a block of FTE hours you may never use. Extra hours you have approved need no new contract.
One agreement covers everything
We prefer to work under one master service agreement: it gives you access to every RecQ service, and you use only the ones you need. We look after the consultants’ contracts, tax and legal requirements in each country.
What happens after you contact us
You send us the outline: phase, indication, countries and timeline.
We reply by the next working day and go through the protocol and the needs of the sites with you on a call.
You get a proposal: the CRAs or consultants we suggest, their experience in similar studies, and the price.
You meet the people before you decide.
One agreement covers the work. We handle the consultants’ contracts, tax and legal requirements.
One contact at RecQ stays with the study for the whole assignment, for you and for the CRA.
RecQ Clinical Consulting
CRAs, start-up specialists, project managers and study managers, freelance or interim. CRA services in Finland
RecQ Nursing
Freelance study nurses and coordinators for screening, study visits, sampling and the eCRF.
RecQ Logistics & Supplies
Transport of study materials and supplies, and travel arrangements for participants.
RecQ Translations
Trial documents into every Nordic language, in the form the Nordic authorities accept.
Archiving
Trial documentation archived after close-out for as long as the regulations require, for example 25 years.
Something not on this list?
Research permits, site agreements or a country-specific hurdle: tell us what is in the way.
Planning a study in Finland or the Nordics?
Tell us about your study: phase, indication, countries and timeline. We reply by the next working day at the latest.
“The cooperation has been excellent: the people at RecQ Clinical are competent, professional, friendly and calm.”
Mikko Kylmänen, Project Manager, Koite Health. Read the client story
