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    Shaping the future of drug development
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Shaping the future of drug development

Software Solutions

Rigorously tested and continuously validated in practice, Cytel software is used at thousands of pharmaceutical, biotech, medical device companies, and leading independent research institutes.

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Cytel’s cutting-edge trial design and implementation expertise, with a specialty in adaptive trials, is helping sponsor companies of all sizes to increase success rates in clinical development.

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Proven product development knowledge and experience from our global multi-disciplinary teams – biostatisticians, operations experts, data managers, programmers and medical writers.

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EUGM 2016

EUGM 2016 Latest News

Just Announced: EUGM March 2016 in Central London

Our annual trial design innovation forum brings together adaptive trial methods and implementation experts from Europe, the US and Asia. Agenda and registration options to be announced soon.

EnForeSys related event

Recruitment Planning with Simulations

Watch Demonstration of EnForeSys®, the Simulations-Guided Feasibility Support Tool

Be truly confident in your trial's enrollment plan: use EnForeSys® to compare recruitment strategies, predict milestones, identify problem areas.

Paris Trial Design Seminar and Training Jan 2016

See Agenda & Registration

Register to Attend the One Day Session on Applying Advanced Methods in Clinical Trial Design

Join regional advanced methods trial design and implementation experts and Cytel's own Bayesian biostatistician Pantelis Vlachos in Paris, January 20th.

What Clients Say

"Cytel’s work on the trial design, simulations and FDA discussions were instrumental in obtaining the regulatory acceptance for our proposed, ground-breaking methodology.

Implementation was smoother thanks to their experience with adaptive population enrichment strategies."

medicines company

--Simona Skerjanec, VP Medical Science
The Medicines Company

"Cytel’s innovative, yet practical adaptive design provided multiple favorable scenarios allowing us stage the Phase 3 VALOR leukemia treatment trial based on sample size re-estimation.

Difficult to imagine our going forward with traditional clinical trial methods alone."


--Steven B. Ketchum, VP Research and Development
Sunesis Pharmaceuticals

"Working with Cytel allowed our team to move forward from research to reality swiftly.

We now have the tools to guide our innovative trial decision-making much more efficiently and knowledgeably."

early stage biostats

--Joe Heyes, VP
Early Stage Biostatistics Merck

"To my knowledge, Fulyzaq® is the very first approved treatment following a two-stage adaptive pivotal study.

There’s no question that without Cytel we wouldn’t have achieved that. You have been very service-oriented and responsive throughout."


--Dr. Scott Harris, CMO
Napo Pharmaceuticals

"We learned controlling critical operational variables with ongoing collaboration – especially between data managers and statisticians – was crucial to trial success.

We even saved 20% by outsourcing the key data analytics, medical writing and submission preparation functions with Cytel."


--Dr. Patrice Rioux, VP, CMO
Raptor Pharmaceuticals

"The Cytel team understood precisely what we needed, and delivered quality work within a very demanding timeframe.

They did it right the first time. As a result, we provided the FDA-requested safety reports without impacting our development timelines."


--Sylvain Nicolas, Global Head Biostatistics Phase 1 Studies

Software Solutions