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With over 25 years of experience, our Phase I flagship site in Warsaw, Poland, has successfully conducted 480+ clinical research projects and completed 74 audits, including 5 FDA inspections with NAI results.
We provide full-service solutions and specialize in:
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Early Phases (FIH, SAD, MAD)
Bioequivalence & biosimilarity
Proof-of-Concept & PK/PD studies
Special populations
Tobacco risk evaluation & smoking cessation
Clinical & non-clinical trial strategy and consulting
Medical writing: Protocols, ICF, CRF, Final Clinical Reports
Regulatory approval support
Project management and study monitoring
Clinical study conduct (including subject reimbursement)
Pharmacokinetics & biostatistics
Bioequivalence & biosimilarity (healthy volunteers & patients)
Proof-of-Concept and food effect studies
Studies involving special populations
First-in-human studies
PK/PD, SAD, MAD
Tobacco risk & smoking cessation studies
With over 20 years of experience and more than 400 completed studies, our team brings extensive practical expertise in conducting and managing clinical research.
Our modern, registered hospital facility covers approximately 2,000 sq. m. and includes treatment and overnight-stay capacity, an infusion room, a Medical Analysis Laboratory and a Hospital Pharmacy with a dedicated cytostatic department.
The site is equipped to support a wide range of protocol requirements, including 12-lead ECG, spirometry, ultrasound, infusion pumps, IMP storage and PK/IMG sample processing. Dedicated refrigerators, -20°C and -70°C freezers, cooled centrifuges, spectrophotometry and access to dry ice further support study-specific laboratory and sample-handling requirements.
Our database includes 12,000 volunteers, with more than 7,500 participants randomized across completed studies, providing an established foundation for recruitment and study delivery.
Our dedicated Patient Engagement function continuously expands participant access through multichannel outreach. We run integrated campaigns across digital and traditional media, including SEO/SEM, targeted social media, educational websites, print, radio and outdoor advertising.
Our experience includes dozens of audits and regulatory inspections, while external certifications, including COBJwDL, support our commitment to rigorous quality standards. We regularly achieve an NPS of over 90. NPS tracking is embedded in our operations, helping us continuously improve the volunteer experience and support retention. Study volunteers frequently highlight the empathy and welcoming atmosphere they experience during their participation, factors that contribute to long-term engagement and peer referrals.
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Over two decades of delivering reliable clinical trial data under strict regulatory oversight.
480 completed studies
7,500+ randomized volunteers
12,000 volunteers in database
2,000 sq. m. registered hospital facility
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Discover how our flexible approach can support your unique study needs.
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