We are Excelya
Excelya is committed to helping clients deliver life-changing therapies through close collaboration. Our global network of experts provides tailored, robust clinical trial solutions across a broad range of therapeutic areas.
We support biotechnology, pharmaceutical, and medical device organizations through flexible Full Service CRO, Functional Service Provider, and Resourcing solutions designed around each clinical development project.
Excelya at a glance
Clinical experts worldwide
Countries covered by our global network
Offices across Europe, Asia, and the United States
Our capabilities help you excel
From protocol design and clinical operations to data management, biostatistics, regulatory support, medical writing, and study reporting, Excelya’s experts provide tailored solutions across the entire clinical development lifecycle. Backed by scientific expertise and operational excellence, our specialist teams help sponsors accelerate development, maintain quality, and achieve successful clinical outcomes.
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
Our solutions meet your needs
We apply the insights and expertise from our decades of local, therapeutic, and service experience to every project. We have a unique business model that means we operate in three modes: Full Service, Functional Service Provider, or Resourcing. This provides the flexibility we need to support your project.
Expert guidance for your clinical trial success, locally and internationally; we collaborate as one team and bring excellence that can help you succeed.
The one-team approach ensures we share responsibility for your outcomes: we can help keep your project on track, on time, and on budget.
Your reliable partner for all clinical research operations role; we will find the right match for you among our large talent pool of experts.
Our Certifications
Our certifications demonstrate Excelya’s commitment to quality, compliance, and operational excellence. They reinforce our expertise in supporting pharmaceutical, biotechnology, and healthcare organizations through trusted standards and continuous improvement.
Certification EcoVadis Bronze
Partenaire de services Veeva
Certification ISO 27001
Frequently Asked Questions
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