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Therapeutic Innovation & Regulatory Science|September 22, 2018
Efficient Source Data Verification Using Statistical Acceptance Sampling: A Simulation StudyRutger M van den Bor, Bas J Oosterman, Martinus B Oostendorp, et al.Therapeutic Innovation & Regulatory Science|September 22, 2018
Interpreting Change in Scores on Patient-Reported Outcome InstrumentsCheryl D Coon, Joseph C CappelleriTherapeutic Innovation & Regulatory Science|September 22, 2018
Risk Management Plans in the European Union: Nonclinical AspectsPaul Baldrick, Lesley ReeveTherapeutic Innovation & Regulatory Science|September 22, 2018
Defining a Central Monitoring Capability: Sharing the Experience of TransCelerate BioPharma's Approach, Part 2Jacqueline Gough, Brett Wilson, Mireille Zerola, et al.Therapeutic Innovation & Regulatory Science|June 28, 2019
What Could the Future of Safety Monitoring Look Like?Steven Hirschfeld, Anne ZajicekTherapeutic Innovation & Regulatory Science|April 17, 2023
Efficient Risk Mitigation Planning for a Clinical TrialVladimir ShnaydmanTherapeutic Innovation & Regulatory Science|April 15, 2023
Complexity of Data Displays in Prescription Drug Advertisements for Healthcare ProvidersJessica Thompson, Molly Lynch, Helen W Sullivan, et al.Therapeutic Innovation & Regulatory Science|April 8, 2023
A Comparison of Instructions for Use Documents and Manufacturer Produced Administration Videos for Biological ProductsVraj Patel, Kellie Taylor, James Schlick, et al.Therapeutic Innovation & Regulatory Science|March 31, 2021
US FDA Drug Approvals are Persistent and Polycyclic: Insights into Economic Cycles, Innovation Dynamics, and National PolicyIraj DaizadehTherapeutic Innovation & Regulatory Science|April 12, 2021
Wearable Technologies for Children with Chronic Illnesses: An Exploratory ApproachFlora McErlane, Elin Haf Davies, Cecile Ollivier, et al.Pageof 165