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Discovery

Our innovative preclinical solutions empower your drug development journey with cutting-edge analytics and insights from inception to preclinical stages.

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Phase I-III Clinical Trials

We help you navigate complex trial phases efficiently with data-driven methods & strategies tailored to Phase I-III trials for accelerated drug development.

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Commercialization

Maximize your market potential and optimize your commercial strategies with our advanced analytical methods, data science, and tailored commercialization solutions for data-driven commercial success.

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Real-World Evidence Solutions

Harness the power of real-world data and real-world evidence to gather insights and shape future drug development cycles for enhanced efficacy and regulatory compliance.

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Clinical Trial Design

Craft optimal trial designs with our advanced analytical methods to enhance efficiency and increase the probability of success throughout your drug’s lifecycle.

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Trial Delivery

Empower your trial delivery by transforming trial designs into actionable strategies with our data-driven approach to ensure seamless delivery and successful outcomes.

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Advanced Analytics

Unlock the power of data with our methods for actionable insights to drive informed decisions and optimize clinical trial outcomes.

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Specialty Areas

We offer tailored analytics solutions for your specialized or niche projects enabling you to optimize both efficiency and precision in drug development.

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Data Strategy Model-lnformed Drug Development Chemistry, Manufacturing and Controls (CMC) Toxicology Solutions Clinical Pharmacology, Drug Metabolism and Pharmacokinetics
Adaptive Trial Designs Complex and Innovative Trial Design Model-lnformed Drug Development Clinical Development Strategy and Planning End-to-End Biometrics Axio® Data Monitoring Committee Data Strategy Regulatory Strategy Market Access Real-World Evidence Software for Trial Design
Health Economics and Outcomes Research (HEOR) Market Access Regulatory Strategy Real-World Evidence Health and Technology Assessments stève consultants
Real-World Evidence Real-World Data Real-World Data Software Post-Authorization Safety Studies stève consultants
Adaptive Trial Design Complex and Innovative Trial design Model-lnformed Drug Development Software for Trial Design
End-to-End Biometrics Data Management Early Phase Solutions Late Phase Solutions Axio® Data Monitoring Committee Safety & Regulatory Compliance FSP Outsourcing Outsourcing per Project Software for Trial Implementation
Systematic Literature Reviews Complex and Innovative Trial Design Market Access Health Economics & Outcomes Research Real-World Evidence Real-World Data Health and Technology Assessments
Synthetic Controls External Controls Rare Diseases Oncology Post-Authorization Safety Studies Decentralized Trials Pediatrics
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Trial Design Software
Trial Implementation and Decision Support Software
LiveSLR® Software for Systematic Literature Reviews
Strategic Consulting

Enhance your clinical trial design with our strategic consulting services, featuring adaptive trial models and comprehensive regulatory guidance to ensure innovative, compliant, and successful trial outcomes.

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Beyond Functional Service Provider

Experience the future of flexible strategic partnerships with Analytics on Demand, providing adaptive and innovative solutions that transcend traditional models to achieve unparalleled operational excellence.

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Project-Based Analytical Solutions

Maximize efficiency and outcomes with our project-based services, delivering specialized expertise, end-to-end biometrics, and focused solutions for unique projects, ensuring timely completion and exceptional results.

Project-Based Analytical Solutions
Trial Design Software

Cytel's software platform enables precise trial design and simulation, utilizing adaptive and Bayesian tools to optimize protocols and accelerate drug development with confidence and efficiency.

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Trial Implementation and Decision Support Software

Our unique software package streamlines trial implementation with intuitive solutions for protocol development, randomization, and patient management, optimizing operational efficiency and ensuring study success.

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LiveSLR® Software for Systematic Literature Reviews

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Adaptive Trial Designs Advanced Analytics Regulatory Strategy Clinical Development Strategy & Planning Discovery and Pre-clinical Clinical Pharmacology, drug metabolism and pharmacokinetics
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Data Management End-to-End Biometrics Data Submission support Axio® Data Monitoring Committee Medical Writing
East Horizon™ Platform for Trial Design Xact software suite, StatXact®
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About Us
About Us

Learn about our rich history, visionary leadership, and core values. Our mission and vision drive us to deliver excellence in drug development globally.

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Explore Cytel’s Insights hub - your source for the latest news, event updates, and expert insights on advanced data analytics and data science.

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Careers

Join our innovative team at Cytel! Explore exciting career opportunities in data science and statistics, analytical methods, and regulatory strategy. Advance the future of human health with us.

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Cytel at ISPOR US

Explore our content hub with everything from booth highlights to presentations and posters.

Our ISPOR 2026 Downloadables

Take a look at our curated selection of white papers and one-pagers, tailored specifically for the ISPOR audience.

Randomized Controlled Trials Aren’t Enough: Why Comparative Effectiveness is the New Strategic Imperative

Discover how to demonstrate comparative effectiveness to differentiate your therapy within saturated markets in this white paper.

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Realizing the Full Value of Integrated Evidence Generation Plan

Understand our approach to better aligning your clinical evidence needs with stakeholder expectations in this one-pager.

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Meet the Presenters

Learn about the talented Cytel team presenting at ISPOR.

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Dalia Dawoud
Dalia Dawoud
Research Principal, HTA Policy and Strategy
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Manuel Cossio
Manuel Cossio
Head of AI Solutions, Real-World Evidence, Value, and Access
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Lilia Leisle
Lilia Leisle
Associate Research Principal, EVA Market Access
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Victor Laliman-Khara
Victor Laliman-Khara
Research Principal, Comparative Effectiveness
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Short Course on May 17th, 8AMright

Prompt Engineering for HEOR: Practical Skills and Use Cases for HEOR Professionals

Dalia Dawoud

May 17 • 8 AM – 12 PM

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Forum on May 18th, 12:15PMright

Living HTA in the Age of AI Innovation: Supporting HTA Decisions at the Speed of Evolving Evidence

Dalia Dawoud and Grammati Sarri

May 18 • 12:15 PM – 1:15 PM

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Forum on May 18th, 3:15PMright

Global Value Frameworks: Aligning HEOR, Access and Policy Across Borders

Dalia Dawoud

May 18 • 3:15 PM – 4:15 PM

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Poster Presentationright

A Pilot Assessment of LLM-Generated Synthetic Cohorts: A First Step Toward Robust Synthetic Control Arms 

Manuel Cossio,  Anupama Vasudevan, and Deepa Jahagirdar  

May 18 • 4 PM – 7 PM 

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Poster Presentationright

Accelerating Dynamic HTA Landscaping in Oncology Through Autonomous Generative AI-Driven Multilingual Data Extraction

Manuel Cossio and Lilia Leisle

May 18 • 4 PM – 7 PM

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Poster Presentationright

Unanchored MAIC vs STC for Binary Outcomes: How Baseline Imbalance Impacts ORR Estimates

Connie Ly and Vikas Jangra

May 18 • 10:30 AM – 1:30 PM

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Poster Presentationright

Assessing the Impact of Missingness in Treatment Effect Modifies on Bias in Anchored and Unanchored MAIC and STC

Victor Laliman-Khara, Mingxin Liu, and Mohammad Sazzad Hasan

May 20 • 9 AM – 11:30 PM

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Our Experts, On Demand

Dive deeper into our insights around AI, RWE, and HEOR with our selection of on demand webinars.

AI in HEOR: Case Studies on Navigating Regulatory and HTA Guidance

Our speakers discuss regulatory and HTA perspectives from different regulatory bodies and provide two use cases for traceable workflows with AI.

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Driving Credibility in External Control Arms with Real-World Data

This webinar explores strategies for selecting, combining, and analyzing diverse data sources to create fit-for-purpose ECAs.

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Featured Blogs

May 14, 2026
A New Frontier in Real-World Evidence: Can AI Create Reliable Synthetic Trial Data?
Manuel Cossio
 ,
Deepa Jahagirdar
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May 5, 2026
How Agentic AI Can Transform HTA Landscaping for EU JCA
Manuel Cossio
 ,
Lilia Leisle
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April 28, 2026
Building a New Evidence Base for Rare Diseases by Structuring Clinical Narratives with Generative AI
Manuel Cossio
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March 26, 2026
Real-World Data Strategies and Challenges: Making Data Work for Your External Control Arm Study
Deepa Jahagirdar
 ,
Vartika Savarna
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