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Medidata: mHealth Can Help in Tracking Patient Outcomes
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Debate Rages Over Placebo Controls in Ebola Trials
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FDA Outlines Clinical Pharmacology Considerations in Pediatric Trials
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Most GCP Infractions Tied to Sponsors, CROs: EMA
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NIH Wants Trial Sites to Use a Single IRB
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India Issues Ream of Clinical Trial Regulations at Year End
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Final Guidance Clarifies Study Data Submission Expectations
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Year in Review: Transparency Leads the Clinical Trial Conversation Again
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FDA Updates Guide on Clinical Study Data eSubmissions
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EMA Publishes GCP Inspection Coordination Procedure
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Australian Details Requirements for Biopharmaceutic Studies
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HHS Panel: Sites Should Provide Trial Results to Patients
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