March 15, 2020
Industry Experience and Perspective on Clinical Trial Safety Reporting to the FDA
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Journal Articles
March 11, 2020
Technology Considerations for enabling eSource in Clinical Research (TIRS)
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March 3, 2020
Accelerating the Adoption of eSource in Clinical Research: A Transcelerate Point of View (TIRS)
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March 1, 2020
SEND harmonization & cross-study analysis: A proposal to better harvest the value from SEND data (Regulatory Toxicology & Pharmacology Journal)
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February 8, 2020
Pharmacovigilance Automation Opportunity – Results from an Industry Survey (Pharmaceutical Medicine)
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February 4, 2020
Investigating Overlap in Signals from EVDAS, FAERS, and VigiBase® (Drug Safety)
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December 28, 2019
Utilizing advanced technologies to augment pharmacovigilance systems: Challenges & Opportunities (DIA TIRS)
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December 10, 2019
Reducing Patient Burden in Clinical Trials Through the Use of Historical Controls: Appropriate Selection of Historical Data to Minimize Risk of Bias (TIRS)
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September 20, 2019
Industry Assessment of the Contribution of Patient Support Programs, Market Research Programs, and Social Media to Patient Safety (DIA TIRS)
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June 18, 2019
Sharing historical trial data to accelerate clinical development (Clinical Pharmacology & Therapeutics)
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