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Clinical Trial Data

 

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The Benefit of Registries for Real-World Evidence Generation in Rare Disease Research

Linda Ross, senior director, peri- and post-approval operations, Evidera, discusses how registries can be an incredibly useful tool in research.

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Infrastructure Design: Key to Enhanced Clinical Trials Data Management

PPD Laboratories experts on PPD's central lab data management service and how it can mitigate challenges throughout a trial.

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Putting Patients First Through Data-Driven Solutions

Gaurav Bhatnagar, VP strategic feasibility, site and patient access, talks data-driven solutions and how they help us focus on patients.

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Randomization Feb 2019

The Do's and Don'ts of Randomization in Clinical Trials

Jolee Graham, biostatistics director, Nicki Payne, director, IRT, and Katy Tam, director, biostatistics, discuss the components of successful randomization in research.

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Balancing Scientific Value and Identification Risk in Anonymization

An overview of anonymization strategy for clinical documents in response to EMA Policy 0043 and Policy 0070

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