Core Business
Accelerate your clinical projects with confidence
Excelya supports medical and clinical development stakeholders in addressing the organizational challenges of a complex, highly regulated, and competitive environment.
As an independent European CRO, we operate across the full lifecycle of medicinal products, from clinical development through commercialization, to help you:
- Limit operational and regulatory risks
- Accelerate critical timelines and time‑to‑market
- Adapt resources to the variability of your projects
- Focus on your strategic priorities
Through our expert teams, proven methodologies, integrated technologies, and flexible delivery models (Resourcing, FSP, Full Service, and more), we sustainably strengthen and scale your clinical and medical organization.
At Excelya, we do more than execute.
We share the risk, so you gain peace of mind, agility, and control over time‑to‑market, without compromise on quality, compliance, or transparency.
Specific Areas of Activity
What do we do?
Excelya is an independent European Contract Research Organization (CRO) specialized in supporting biotechnology, pharmaceutical, and medical device companies across the full lifecycle of medicinal products, from clinical development through commercialization. We provide Full-Service CRO, Functional Service Provider (FSP), Resourcing, and integrated clinical development solutions, supported by expert teams in clinical operations, biometrics, pharmacovigilance, regulatory affairs, medical writing, and medical affairs across a wide range of therapeutic areas.
For what type of studies?
Excelya expert teams have conducted a large number of Phase I to IV trials for drugs, medical devices or combined drugs and devices as well as Phase IV / NIS non interventional studies/ IS, Real-World Evidence (RWE) studies and Commercial optimization.
Our goal: to deliver on-time, on-budget and on-quality clinical research enhanced by the commitment, passion and innovative mindset of our expert and project teams.
Who are our clients?
Excelya works for Pharmaceutical Companies, Biotechs and medical device organizations on some of the most innovative drug candidates and disruptive drug delivery technology. Excelya has been working for MedTech, Big Pharma and Biotechs in their Medical Device development program and In-Vitro Diagnostic Devices.
Key areas of focus
Clinical trial management – Data Management – Early Clinical Phases – eCRF – Information – Investigator Network – Late phase IV – Legal Representation – Medical Advising – Medical Writing – People selection & placement – Pharmacovigilance & Drug – Project Management – Regulatory – Safety – Statistics – Translation
Sales Representative
Mihael Mironov
Sr Managing Director
[email protected]
+32492588184
