Integrated clinical trial delivery
in Northern Europe
CTC combines full-service CRO capabilities with an in-house
Site Network across Sweden and the Netherlands.
CRO and sites, working as one
Clinical trials often require sponsors to coordinate CRO teams, recruitment providers and independentsites. Each additional interface introduces another dependency.
At CTC, clinical operations, recruitment, monitoring, data, safety and site delivery are connected withinone organisation. This enables closer coordination across the study and provides sponsors with onepartner across clinical trial delivery.
Clearer oversight
CRO and site teams work within a shared operational structure.
Fewer handovers
Recruitment, clinical conduct and study oversight are coordinated from the start.
Direct clinical capacity
Access professional research units across Sweden and the Netherlands through one network.
From first dose to decision-ready data
Early development decisions depend on more than successful clinical conduct.
CTC combines study design, clinical pharmacology, hospital-based First-in-Human conduct, biometricsand reporting to support sponsors from protocol development to interpretable study results.
Our dedicated First-in-Human unit is located at Uppsala University Hospital and provides access toexperienced medical teams and hospital infrastructure.
Relevant capabilities include:
First-in-Human, SAD and MAD studies
Clinical pharmacology and PK/PD support
Hospital-based clinical conduct
Medical and safety oversight
Biometrics and clinical reporting
Recruitment built into delivery
Recruitment risk is rarely solved by site selection alone.
CTC connects recruitment strategy, patient access, pre-screening, medical expertise and clinical siteoperations. Recruitment activities are aligned with the protocol, study timelines and available clinicalcapacity from the beginning.
Our model combines:
- Central recruitment capabilities
- Participant databases and targeted advertising
- Structured pre-screeningAccess to relevant patient populations and medical specialists
An integrated Site Network
CTC operates seven professional research units across Sweden and the Netherlands, combining morethan 70 in-patient beds with high out-patient capacity.
The network supports early-phase studies, patient trials, multicentre studies and medical deviceinvestigations.
Seven research units
Across Sweden and the Netherlands
70+ in-patient beds
Combined with high out-patient capacity
Integrated recruitment
Patient access, pre-screening and clinical conduct
One delivery model
CRO services and sites within one organisation
Why CTC?
CTC stands out by its in-house Site Network with 6 state-of-the-art research clinics across Sweden, including a FIH unit at Uppsala University Hospital, and an additional clinic in the Netherlands.
We provide full-service management and conduct of Phase 0, FIH, Phase I and Phase II studies as well as medical device investigations. Our site network supports clinical trials in all phases of development. With a flexible and innovative mindset, we offer a streamlined, cost-effective, and optimised solution customised for each trial.
We translate science into treatment.
With patients for patients – rethinking clinical trials.
Let’s discuss your upcoming study
Whether you are planning a First-in-Human programme, evaluating European sites or looking tostrengthen recruitment, CTC can assemble the relevant clinical, scientific and operational expertisearound your study
Phone: +46 (0) 18-30 33 00
Email: rfp@ctc-ab.se
Reach out to us via the form if you have any questions, inquiries or RFPs.