Clinical Biostatistics
Study design, analysis and reporting across clinical development, from early phase through submissions.
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Statistical and regulatory support for pharmaceutical and biotech teams, from early development through to submission and beyond.
Sound analysis. Practical insight.Real-world impact for complex development and regulatory decisions.
Quality
Robust methods, careful review and documentation appropriate to regulated work.
Rigour
Experienced statistical judgement applied to complex development questions.
Trust
Direct senior involvement, clear communication and dependable delivery.
Our Services
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CMC Statistics
Statistical support for process development, characterisation, validation, stability and lifecycle work.
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Regulatory Analytics
Analysis and evidence support for submissions, regulatory questions and lifecycle changes.
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Data & Product Engineering
Data systems, analytics and tools to support regulated decision making at scale.
Learn moreOur Leadership
Senior expertise at every stage of development.
EndPointScience is a specialist statistical consultancy founded by biostatistician Halima Boutouil. Specialising in [verified disciplines], the practice supports pharmaceutical and biotech teams across [verified areas/stages]. Clients work directly with senior specialists throughout each engagement, from planning and analysis through to reporting, submission support and lifecycle work.
Our focus is simple: to provide clear, rigorous and practical statistical and regulatory support that helps our clients bring important therapies to patients.