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Resource Library

Welcome to our resource library, a comprehensive collection of eBooks, white papers, case studies, on-demand webinars, and more.  

Four decades of thought leadership, deep academic roots, and strong alliances with industry experts enable us to offer unique insights into every aspect of the ​drug development cycle.

Explore our full range of resources to enhance your understanding of the therapy-defining power of data analytics and how they can help you make better-informed decisions, no matter where you are on your path to achieving improved patient outcomes.

Asset type
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Whitepapers
Webinars
eBook
Case Studies

Drug development Phases
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Preclinical
Phase 3
Phase 2
Phase 1

Service type
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Synthetic Controls
Submissions
Strategic Consulting
stève consultants
software
SLR
Simulations
RWE
RWD
Regulatory Affairs
Post-Marketing
Pediatrics
PBS
PASS
Optimization
Observational Study
Modeling
IRA
HTA
HEOR
FSP
External Controls
EVA
Epidemiology
East Horizon
East
East
Early Phase
Dose-Finding
Database Study
Data Monitoring Committees
Cost-effectiveness
Comparative Study
Biostatistics
Biometrics
Bayesian
AI
Adaptive Trial Design

Therapeutic Areas
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Respiratory Diseases
Rare diseases
Oncology
Neurolomuscular Disorder
Neurological Disorder
Metabolic Disorders
Macular Degeneration
Liver Disease
Infectious Diseases
Cardiovascular
Blood Disorder
Autoimmune Disease
White Paper – Leveraging Cloud Computing and Advanced Software for Parameter Optimization of Multi-Arm Multi-Stage Designs
December 17, 2025
White Paper – Leveraging Cloud Computing and Advanced Software for Parameter Optimization of Multi-Arm Multi-Stage Designs
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Case Study – Accelerating Chronic Pain Treatments Through Optimal Interim Analyses Timing in Adaptive Clinical Trial Design
November 7, 2025
Case Study – Accelerating Chronic Pain Treatments Through Optimal Interim Analyses Timing in Adaptive Clinical Trial Design
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October 16, 2025
Webinar – Rethinking Clinical Trials in Early Development: How External Controls Drive Ethical, Efficient Development
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Case Study – Tailoring Statistical Services for Academic Clients and Unlocking Greater Value for Medical Research
October 16, 2025
Case Study – Tailoring Statistical Services for Academic Clients and Unlocking Greater Value for Medical Research
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October 15, 2025
White Paper – Randomized Controlled Trials Aren’t Enough Why Comparative Effectiveness is the New Strategic Imperative
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October 9, 2025
Webinar – Leveraging the Right Advanced Quantitative Methods to Address Evidentiary Gaps
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September 24, 2025
Webinar – The Role of Real-World Evidence in Addressing Post-Launch Needs
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September 17, 2025
Webinar – Boosting Efficiency with CRF and CDISC Standards
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September 16, 2025
Webinar – FDA’s Project FrontRunner: Reshaping Oncology Drug Development
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September 10, 2025
Webinar – Boosting Phase III Probability of Success with Informed Priors from Phase II Data
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September 2, 2025
White Paper – Navigating the Evolving Landscape of Data Engineering and the Quest for Elusive Talent
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White Paper – Optimizing Interim Analyses Considering Potential Enrollment Variations: A Cytel-GSK Trial Design Case Study
September 1, 2025
White Paper – Optimizing Interim Analyses Considering Potential Enrollment Variations: A Cytel-GSK Trial Design Case Study
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Book a free, 30-minute 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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