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Drug Development Cycle
Discovery
Phase I-III Clinical Trials
Commercialization
Real-World Evidence Solutions
Strategic Data Science and Analytical Methods
Clinical Trial Design
Trial Delivery
Advanced Analytics
Specialty Areas
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
Delivery Models
Strategic Consulting
Beyond Functional Service Provider
Project-Based Analytical Solutions
Software Solutions
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
Staff Augmentation Strategic Capacity Management Functional Service Provider Hybrid FSP Model
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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Insights

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
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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Clinical Trial Delivery

Transform designs into actionable strategies with our data-driven approach. By seamlessly integrating our analytical methods, we empower you to deliver successful outcomes and accelerate the drug development process. 

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Trial Delivery

Our Trial Delivery Services

Cytel’s comprehensive trial delivery solutions enable you to follow a seamless journey from concept to commercialization. Our integrated approach encompasses every aspect of clinical development, from early-phase studies to late-phase trials, biometrics, data monitoring, and more. With customized strategies and expert support, we optimize study design, enhance data quality, and accelerate timelines to deliver impactful results. Trust in our proven expertise and innovative solutions to navigate the complexities of trial delivery and bring your treatments to market efficiently and effectively. 

Our Solutions

End-to-End Biometrics

Harness the power of biostatistics, statistical programming, medical writing, and data management to optimize trial design, data analysis, and reporting to ensure robust results and regulatory compliance throughout your clinical development journey.

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Early-Phase Solutions

Accelerate your product's journey from bench to bedside with our early-phase solutions. From first-in-human studies to proof-of-concept trials, we offer comprehensive strategies to optimize study design, mitigate risks, and lay the groundwork for successful development.

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Late-Phase Solutions

Unlock the full potential of your drug’s lifecycle with our late-phase solutions. From regulatory submissions to market access planning and post-marketing commitments, we provide tailored strategies to maximize market success and patient impact.

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Safety and Regulatory Compliance

Many drug development projects fail due to constraints in time and funding. We help you define your regulatory strategy early during development, increasing the chances of doing the right thing at the right time. 

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Outsourcing with our Functional Service Provider Solutions

Beyond traditional FSP models, Cytel offers innovative solutions tailored to meet unique project needs, providing flexible and comprehensive support throughout the drug development lifecycle.

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Axio® Data Monitoring Committee

Our vigilant oversight of trial data identifies trends, anomalies, and potential issues, ensuring integrity throughout. Data monitoring committees, with our Axio unit, ensure regulatory compliance and patient safety, fostering trust in clinical trial outcomes.

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Outsourcing Per Project

Cytel delivers customized project-based solutions, addressing your specific needs and challenges with efficiency and expertise, and ensuring successful outcomes in every stage of the drug development process.

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Data Management

Our data management solutions seamlessly orchestrate your trial data, ensuring accuracy, completeness, and regulatory compliance from collection to analysis.

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Software for Trial Implementation

Our software packages facilitate seamless trial implementation, offering intuitive solutions for protocol development, randomization, and patient management to optimize operational efficiency and ensure study success.

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100%

Acceptance of Study Designs by FDA

>6,000

Phase I-IV Trials in the last 10 years

69

2024 Net Promoter Score, reflecting outstanding client satisfaction.

Claim your free 30-minute strategy session

Book a free, no-obligation strategy session with a Cytel expert to get advice on how to improve your drug's probability of success and plot a clearer route to market.

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