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Why is there such inefficiency in site selection?
December 15, 2016
CenterWatch Staff
Why we need to redefine the “team” in rare disease trials
December 1, 2016
CenterWatch Staff
Engaging patients for a more successful clinical trial
November 15, 2016
CenterWatch Staff
Pharma and CROs turn to risk-sharing to improve trial performance
November 1, 2016
CenterWatch Staff
Fueling mHealth adoption to bridge the communications gap
October 15, 2016
CenterWatch Staff
Heterogeneity and precision medicine: An integrated approach
October 1, 2016
CenterWatch Staff
Don’t let noncompliant patients damage your clinical trial
September 1, 2016
CenterWatch Staff
Benefits for international multicenter clinical trials in Russia
September 1, 2016
CenterWatch Staff
The importance of multifaceted virtual investigator meetings
August 15, 2016
CenterWatch Staff
To treat rare diseases, every patient counts
August 1, 2016
CenterWatch Staff
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Upcoming Events
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Effective Root Cause Analysis and CAPA Investigations for Drugs, Devices and Clinical Trials
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21
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MAGI@home Clinical Research Conference 2024
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Surviving an FDA GCP Inspection: Resources for Investigators, Sponsors, CROs and IRBs
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Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials
The information you need to adapt your monitoring plan to changing times.
Learn More Here