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Solutions

Our solutions, powered by intelligence, enable confident decisions – from Phase I to market.

Software

Cytel’s award-winning statistical and predictive software solutions enable our clients to make the best possible decisions. Our software portfolio offers adaptive, Bayesian, and exact tools which allow you to go fast and learn as you go.

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Solara

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Solara combines over 30 years of Cytel’s insight and advanced analytics expertise with the infinite power of cloud computing in a new platform that redefines clinical trial development. 

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East

East® provides users with a wide range of features, including sample size and power calculation tools, adaptive features planning, a trial monitoring dashboard, advanced simulations to test hypotheses before experimental implementation, and text-book-quality documentation and access to support from world-renowned statistical experts. 
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East Bayes

Cytel is bringing you East Bayes a web-based extension of East for clinical trial design that blends the pace of SaaS delivery, the ease of use and robustness of Cytel software, and the velocity of cloud-based computing.

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Xacts

StatXact provides the world’s most comprehensive toolkit for such analyses, offering more than 150 tests and procedures into a validated software package.
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Trial Implementation Software

Cytel’s experts have over three decades worth of experience in building technology for clinical trial success.

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Real World & Advanced Analytics

Through our advanced analytics, Cytel provides the richer, deeper insights necessary for making confident development decisions. We generate evidence which complements traditional randomized clinical trials, accelerates submissions, expands indications, and supports health-economic decision-making.

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Work with us to unlock the full potential of your data

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Health Economics & Outcomes Research

Cytel’s experts in Health Economic Outcomes Research generate evidence-based cost-effectiveness models that showcase the true economic value of your product. They specialize in health economic modeling, HEOR value communication, and other standard models of pharmaceutical modeling for comparative effectiveness research.

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Real World Evidence

Cytel’s experts in Real World Evidence use advanced quantitative techniques to prepare sponsors for regulatory submission and market access.

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Head-to-Head

Two therapies are placed in head-to-head clinical trials when they are compared against each other as opposed to a standard of care.

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Synthetic Control Arms

The increased use of single arm trials in oncology and rare diseases to augment clinical trial submissions requires specialized statistical knowledge particular of Bayesian statistical methods.

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Global Health

Cytel’s experts in Global Health work with policy-makers, philanthropists and other geopolitical stakeholders to ensure that low- and middle-income countries (LMICs) benefits from the scientific developments in global biopharma.

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Innovative Trial Design

Cytel is the largest provider of statistical software and advanced analytics for clinical trial design and execution. Our clients have the tools and expertise they need to design the best possible clinical trials,  providing promising results for all patient populations, as quickly and efficiently as possible.

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Complex Innovative Designs

Clinical trials with advanced innovative designs use adaptive methods, Bayesian methods and other novel clinical trial design techniques to increase efficiency and reduce costs.

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Analytics in Design

Cytel's expert statisticians, data scientists and quantitative strategies will help you to reveal the full potential of your clinical studies. Prepare for submission with a strong quantitative data strategy.

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Solara

Solara combines over 30 years of Cytel’s insight and advanced analytics expertise with the infinite power of cloud computing in a new platform that redefines clinical trial development. 

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Biometrics Implementation

Cytel’s modern approach to resourcing is based on the simple premise that every customer deserves the “A” team. Whether you face a complex statistical issue, or the need for knowledgeable collaborators to handle biometrics and trial implementation, Cytel has skilled professionals available when you need them.

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Full Service Biometric Solutions

Whether you are a global pharmaceutical company or a virtual biotech, you deserve the dedicated and experienced A-team that can ensure that your projects are executed accurately, on-time and on-budget.

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Early Phase Solutions

As sponsors prepare to explore the full potential of a new product, they need a team known to reveal product value with swift delivery and precise execution.
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Late Phase Solutions

With the goal of demonstrating safety and effectiveness of a therapy we expect the sponsor to insist that the clinical trial implementation team executes a trial with efficiency, precision and expertise.

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Axio Data Monitoring Committee

At Cytel, we know that you entrust your Data Monitoring Committee (DMC) with a great deal of responsibility, often at the most critical stages of clinical development. We are here to protect the integrity of your clinical trial.

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Regulatory Submission Support

As a registered solutions provider of the Clinical Data Interchange Standards Consortium (CDISC), Cytel’s regulatory submissions teams are well-versed in the clinical data submission models that regulators are coming to expect in their clinical trial assessments.

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Functional Service Provision

Cytel takes pride in offering our clients access to teams that can act as extensions of a sponsor’s permanent staff. We bring a proven methodology that helps us identify, onboard and deploy talent to your team at both a local and global level, depending on your trial’s needs.

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Disciplines

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Health Economics

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Showcasing the full value of a product through masterful comparative effectiveness studies, evidence generation, and more.

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Data science

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Sophisticated techniques for assessing data quality, analyses and evidence generation.

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Biostatistics

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Advanced methods for innovative clinical trial design including adaptive methods, Bayesian techniques, population enrichment, digital biomarkers and more.

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Statistical programming

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Ensuring that biometrics for classical and novel clinical trial designs are enhanced with knowledgeable statistical techniques and proven delivery.

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Medical Writing

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Crafting the narrative that illuminates the full value of new products.

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Epidemiology

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Modeling disease progression for local, national and international governments and a significant portfolio in LMICs and global health.