March 29, 2021
Protocol Deviations: A Holistic Approach from Defining to Reporting (TIRS)
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Journal Articles
March 19, 2021
Pandemic Response Ushers in New Era of Biopharma Data Sharing (BioCentury)
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February 1, 2021
Validating Intelligent Automation Systems in Pharmacovigilance: Insights from Good Manufacturing Practices (Drug Safety)
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December 20, 2020
Leveraging the Value of CDISC SEND Datasets for Cross-Study Analysis: Incidence of Microscopic Findings in Control Animals (Chemical Research in Toxicology)
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September 3, 2020
Quality Tolerance Limits: Framework for Successful Implementation in Clinical Development (TIRS)
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July 20, 2020
Evaluation of the Content Validity and Cross-Cultural Validity of the Study Participant Feedback Questionnaire (SPFQ) (TIRS)
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July 2, 2020
“Amplifying the Voice of the Patient in Clinical Research: Development of Toolkits for Use in Designing and Conducting Patient Centered Clinical Studies (TIRS)
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May 29, 2020
Patient preferences when searching for clinical trials and adherence of study records to ClinicalTrials.gov guidance in key registry data fields (PLOS One)
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April 1, 2020
Safety Analytics Best Practice Considerations
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March 15, 2020
Industry Experience and Perspective on Clinical Trial Safety Reporting to the FDA
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