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Successful Application of Intelligent Monitoring Tools in Data Management Risk-based monitoring and reduced source document verification offer a new approaches to running better clinical trials, making them two of today's most talked about topics among research organizations. These developments make data management more important than ever. Are we fully using our data to drive processes, to inform our decisions, and proactively prevent issues in our clinical trials?
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With 11,000+ employees covering 80+ countries, PRA Health Sciences delivers phase I-IV global, drug development solutions across a broad range of therapeutic areas.
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Change Investigation Site Relationships for the better
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ACT TV
Tune in to ACT TV, our new video channel, features regular interviews with experts on popular topics in clinical trials, and drug development. Programming includes Listening to Social Media, eConsent, Orphan Drugs, Risk-Based Monitoring and more.
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