Excelling with care

 

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.

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Excelya at a glance

900+
 

Clinical  experts worldwide

40+
 

Countries covered by our global network

13
 

Offices across Europe, Asia, and the United States

Excelya the CRO

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
Pharmacovigilance
Data Management
eTMF Management
Medical Affairs
Statistics & Programming
Regulatory Affairs

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

Discover Clinical Operations

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

Explore Pharmacovigilance & Safety

Data Management

 
 

Capitalize on effective data management with support from our dedicated global data management team of experts committed to privacy, security and excellence.

90+

Studies since 2022, over the last 4 years

3/5

Top leading EDC systems supported

Discover Clinical Data Management

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


Explore eTMF Management

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

Discover Medical Affairs

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

Explore Statistics & Programming

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

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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.

Full Service   
 
 


Expert guidance for your clinical trial success, locally and internationally. We collaborate as one team and bring excellence that can help you succeed.  

    Discover FS Model →  

FSP
 
 


The one-team approach ensures we share responsibility for your outcomes. We help keep your project on track, on time, and on budget.

    Explore FSP Partnership →

Resourcing  
 
 


Your reliable partner for all clinical research operations roles. We will find the right match for you among our large talent pool of experts.

Explore Resourcing Solutions →  

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.

Badge de certification EcoVadis Bronze

Certification EcoVadis Bronze

Recognition & professional growth

Badge Partenaire de services Veeva

Veeva Service Partner

Expertise & service excellence

 

Badge de certification ISO 27001

Certification ISO 27001

Learning & achievement showcase

Excelya_Worldwide_CRO_Accross_40+_Countries

Frequently Asked Questions

 

What makes Excelya different as a CRO partner?

Excelya combines global scale with a lean mid size approach, giving you senior attention, fast decisions, and flexible delivery across your portfolio

What values guide how Excelya works with clients?

Audacity, Care, and Energy shape how teams work every day, with proactive problem solving, strong ownership, and a people first mindset

How strong is Excelya’s global coverage and delivery capability?

Excelya has 1000 plus experts, 16 offices, and coverage across 25+ countries, combining local execution with global coordination

What proof is there of real clinical delivery experience?

Excelya has run 550 plus clinical trials across early phase, Phase I to IV, and late phase studies, covering many therapeutic areas

Stay Ahead with our Experts

 

Let’s solve your challenges together

 

Submit your request