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Therapeutic Innovation & Regulatory Science|November 26, 2021
Clinical Development and Regulatory Pathways of Monoclonal Antibodies in JapanHua Liao, Zhaoyang LiTherapeutic Innovation & Regulatory Science|January 13, 2022
Anti-lung Cancer Marine Compounds: A ReviewMohammad Reza Miri, Afshin Zare, Jamileh Saberzadeh, et al.Therapeutic Innovation & Regulatory Science|October 14, 2022
Considerations for Embedding Inclusive Research Principles in the Design and Execution of Clinical TrialsUbong Peters, Brenna Turner, Daniel Alvarez, et al.Therapeutic Innovation & Regulatory Science|October 31, 2022
Bayesian Method of Borrowing Study-Level Historical Longitudinal Control Data for Mixed-Effects Models with Repeated MeasuresHong Li, Man Jin, Yu-Che Chung, et al.Therapeutic Innovation & Regulatory Science|October 21, 2022
Does Central Monitoring Lead to Higher Quality? An Analysis of Key Risk Indicator OutcomesSylviane de Viron, Laura Trotta, William Steijn, et al.Therapeutic Innovation & Regulatory Science|October 24, 2022
Sample Sizes Using Hochberg's Procedure for Two Comparisons with Three Different Study DesignsDavid R BristolTherapeutic Innovation & Regulatory Science|October 4, 2022
Navigating Medical Device Certification: A Qualitative Exploration of Barriers and Enablers Amongst Innovators, Notified Bodies and Other StakeholdersRebecca Baines, Petra Hoogendoorn, Sebastian Stevens, et al.Therapeutic Innovation & Regulatory Science|August 27, 2022
Leveraging Patient Preference Information in Medical Device Clinical Trial DesignLiliana Rincon-Gonzalez, Wendy K D Selig, Brett Hauber, et al.Therapeutic Innovation & Regulatory Science|January 10, 2022
Maximizing Regulatory Review Efficiency: The Evolution of the FDA OCE RTOR PilotYa Grace Gao, Samantha Roberts, Allison GuyTherapeutic Innovation & Regulatory Science|January 10, 2022
The Occurrence of Encephalitis Due to Immune Checkpoint Inhibitors: A Pharmacovigilance StudyYugo Chisaki, Hiroki Hata, Chikako Matsumura, et al.Pageof 165