Our capabilities help you excel
Our experts can support you on key tasks from protocol design to final report. Excelya’s specialist teams have a wide range of capabilities, helping you achieve excellence throughout your clinical projects.
Clinical Operations
Overcome obstacles and ensure your clinical trial runs smoothly, from early phase to late phase development. Benefit from our international reach and global network of experts.
400+
Clinical projects delivered
16%
Cost Reduction
Pharmacovigilance
Strengthen your pharmacovigilance with people who have academic backgrounds, deep knowledge of legislation, and years of hands-on experience.
20+
Pharmacovigilance expertise
24/7
Drug safety monitoring
Data Management
Capitalize on effective data management with support from our dedicated global data management team of experts dedicated to privacy, security and excellence.
90+
Studies since 2022, over the last 4 years
3/5
top Leading EDC systems supported
eTMF Management
Get your study ready for submission with our best-in-class processes, procedures and implementation experience, delivered by our industry-leading team.
100% Digital
Trial document management
3+ Years
Average clinical trial experience
Medical Affairs
Fully optimize your study documents and put your findings into words with our expert Medical Affairs, Medical Writing, and Publishing teams.
100+ Experts
Medical writers & affairs professionals
100+
Publications Peer-reviewed papers delivered
Statistics & Programming
Gain insights that accelerate decision-making and improve the quality of submissions: let our biostatistics experts take care of your statistics, from protocol design to analyzing results.
150+ Experts
Biometrics specialists
25+ Years
Longest client partnerships
Regulatory Affairs
Navigate complex regulatory requirements, strengthen compliance and support faster market access: our regulatory affairs experts guide your products across strategy, submissions and lifecycle management.
3 Pillars
Strategy, submissions, lifecycle
360°
Regulatory support
EXCELYA SOLUTIONS
Flexible CRO Solutions for Clinical Development
Choose the right level of clinical research support with Excelya’s Full Service, Functional Service Provider (FSP) and Resourcing solutions.
01
COMPLETE TRIAL DELIVERY
Full Service CRO
End-to-end clinical trial management through integrated scientific, operational and regulatory expertise. Excelya coordinates clinical development activities with a focus on quality, collaboration and efficient delivery.
✓ Integrated clinical trial management
✓ Multidisciplinary expertise
✓ Coordinated project delivery
02
DEDICATED FUNCTIONAL TEAMS
Functional Service Provider
Dedicated clinical development expertise through a flexible FSP model. Excelya provides specialist teams that integrate with sponsor operations while supporting selected functions and evolving project requirements.
✓ Dedicated functional expertise
✓ Scalable specialist teams
✓ Flexible operational support
03
FLEXIBLE CLINICAL EXPERTISE
Clinical Resourcing
Strengthen existing clinical research teams with qualified professionals. Excelya’s Resourcing model provides specialist expertise that integrates into sponsor organisations and supports changing operational needs.
✓ Qualified clinical professionals
✓ Integration with sponsor teams
✓ Flexible resource allocation
ABOUT EXCELYA
An Independent European CRO
Excelya supports pharmaceutical, biotechnology and medical device companies with flexible clinical research solutions. Our multidisciplinary teams combine scientific expertise, operational experience and a collaborative approach to support sponsors throughout clinical development.
Find the Right Clinical Research Solution
Explore how Excelya’s Full Service, FSP and Resourcing models can support your clinical development priorities.