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Pharmaceutical Medicine|September 3, 2021
Leveraging Case Narratives to Enhance Patient Age Ascertainment from Adverse Event ReportsPhuong Pham, Carmen Cheng, Eileen Wu, et al.Pharmaceutical Medicine|June 20, 2020
Evolving Communication with Healthcare Professionals in the Pharmaceutical Space: Current Trends and Future PerspectivesAndriy Krendyukov, Dévi NasyPharmaceutical Medicine|December 1, 2022
Evaluating Treatment Efficacy by Combining Multiple Measures in Clinical Trial ApplicationsAbdullah Al Masud, Samaradasa Weerahandi, Ching-Ray YuPharmaceutical Medicine|December 17, 2022
Somatic Gene Therapy Research in Pediatric Populations: Ethical Issues and Guidance for Operationalizing Early Phase TrialsAlison Bateman-House, Lesha D Shah, Rafael Escandon, et al.Pharmaceutical Medicine|January 18, 2023
Digital Therapies (DTx) as New Tools within Physicians' Therapeutic Arsenal: Key Observations to Support their Effective and Responsible Development and UseJean-Christophe Bélisle-Pipon, Pierre-Marie DavidPharmaceutical Medicine|July 5, 2021
Preparing for the Next Normal: Transformation in the Role of Medical Affairs Following the COVID-19 PandemicRomik Ghosh, Senthilnathan Mohanasundaram, Sujatha Shetty, et al.Pharmaceutical Medicine|July 22, 2021
Evaluation of Drug Lags in Development Initiation, New Drug Application and Approval Between Japan and the USA and the Impact of Local Versus Multi-regional Clinical TrialsSatoshi Ushijima, Naoki Matsumaru, Katsura TsukamotoPharmaceutical Medicine|March 13, 2022
Medical Affairs and Innovative Medicinal Product Strategy DevelopmentAndriy Krendyukov, Dévi NasyPharmaceutical Medicine|March 6, 2022
Medical Affairs Transformation in Specialty Pharma: Next-Level Collaboration at the CoreAntony Fulford-Smith, Emma Leah, Anie Azroyan, et al.Pharmaceutical Medicine|February 4, 2021
The Qualitative Value of Facilitated Regulatory Pathways in Europe, USA, and Japan: Benefits, Barriers to Utilization, and Suggested SolutionsMagdalena Bujar, Neil McAuslane, Lawrence LibertiPageof 31