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S. Faye Williamson

Medicines and Healthcare products Regulatory Agency’s “Consultation on proposals for legislative changes for clinical trials”: a response from the Trials Methodology Research Partnership Adaptive Designs Working Group, with a focus on data sharing
Subgroup analyses in randomized controlled trials frequently categorized continuous subgroup information
Bayesian sample size determination for diagnostic accuracy studies
Generalisations of a Bayesian decision-theoretic randomisation procedure and the impact of delayed responses

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