Statistical Consultants for Clinical Trials | CRO

Clinical trial planning, design, and analysis

PHASTAR can support the planning, design and analysis of your clinical trial programme. Regardless of the complexity of your project, PHASTAR can provide expert statistical solutions and experienced technical advice, tailored to meet your needs.

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Our services include

Statistical input into study design & protocol development
Adaptive study designs
Sample size calculations
Analysis plans
Optimising study success
Identifying the primary endpoint
Modelling and simulation
Prediction of drug exposure
Optimal evaluation of information for on-going clinical trials

Independent data monitoring committees
Setting up randomisation schemes
Multiplicity (optimally evaluate more than one outcome in a trial)
Regulatory advice
Observational and epidemiological studies
Interpretation of results
Data visualisation
Statistical training

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Independent data monitoring committees

PHASTAR offers sponsors seamless support for Independent Data Monitoring Committees, through expert advice and support, agile and adaptable approach to systems and logistical expertise.

For more information on IDMCs click here.

Expert study design, statistical analysis, data science, data capture, and reporting for clinical trials

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Email: This email address is being protected from spambots. You need JavaScript enabled to view it.

Tel UK: +44 (0)20 7183 7062
Tel US: +(1) 646 851 2624

UK HQ: 2D Bollo Ln, Chiswick,
London, W4 5LE

US HQ: 300 w. Morgan street suite 120,
Durham, NC, 27701