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Clinical trial design and data collection and analysis form an integrated process that ensures reliable, valid evaluation of investigational treatments; rigorous protocol development defines objectives, endpoints, eligibility criteria, randomization and blinding methods, and statistical power to minimize bias and protect participant safety.
Clinical trial design and data collection and analysis form an integrated process that ensures reliable, valid evaluation of investigational treatments; rigorous protocol development defines objectives, endpoints, eligibility criteria, randomization and blinding methods, and statistical power to minimize bias and protect participant safety.