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Monthly Features
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Tracking adoption of risk assessment and RBM
October 1, 2017
CenterWatch Staff
FDA Fast Track designations reach 20th year
October 1, 2017
CenterWatch Staff
Is eConsent adoption poised to grow?
September 1, 2017
CenterWatch Staff
Site selection a continuing conundrum
September 1, 2017
CenterWatch Staff
Preparing sites for post-acquisition integration
August 1, 2017
CenterWatch Staff
Fastest drug developers and their practices
August 1, 2017
CenterWatch Staff
Revisiting patient diversity in clinical trials… again
July 1, 2017
CenterWatch Staff
Preparing sites for acquisition
July 1, 2017
CenterWatch Staff
Assessing the strategic impact of supply chain management
June 15, 2017
CenterWatch Staff
Electronic Health Records gain ground in clinical research
June 1, 2017
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
14
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2024 Avoca Quality Consortium Summit
Featured Products
Surviving an FDA GCP Inspection: Resources for Investigators, Sponsors, CROs and IRBs
Best Practices for Clinical Trial Site Management
Featured Stories
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Ask the Experts: Applying Quality by Design to Protocols
Clinical Trials Need Greater Representation of Obese Patients, Experts Say
FDA IT Modernization Plan Prioritizes Data-Sharing, AI, Collaboration and More
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