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Pharmaceutical Medicine|June 6, 2026
An Expert Consensus-Based Review of Considerations for Developing a Quality Management System Framework for Studies Utilising Secondary Data for Real-World Evidence GenerationDeborah Layton, Antonella Porta, Dony Patel, et al.
Pharmaceutical Medicine|January 9, 2024
Rare Immune-Related Adverse Events (irAEs): Approach to Diagnosis and ManagementAnadil Javaid, Catherine Bennett, Aparna Rao, et al.
Pharmaceutical Medicine|June 22, 2026
A Framework for Standardising Toxicity Management Guidelines in Oncology Clinical TrialsSanjana Singarayer, Heidi Lloyd-Williams, Abigail Morrison, et al.
Pharmaceutical Medicine|October 8, 2020
Proposal of Standard for Medical Science Liaison (MSL) Profession in Japan: A Viewpoint from the Japanese Association of Pharmaceutical Medicine (JAPhMed)Michiko Tomiyasu, Kunihiko Hayashi, Yukio Moritsugu, et al.
Pharmaceutical Medicine|July 20, 2026
The Impact of Clinical Trial Participation on Quality of Life in Duchenne Muscular DystrophyAidan W Leffler, Graham J Leffler, Marielle G Contesse
Pharmaceutical Medicine|August 10, 2026
Integrated Evidence Generation Planning: Why Medical Affairs is a Critical PartnerRonaldo Fujii, Masoud Nouri, Mohammad Khan, et al.
Pharmaceutical Medicine|August 19, 2026
Impact of Regional Healthcare Policy Interventions on Biosimilar Use: A 10-year Evaluation of TNFα Inhibitors Utilization in ItalyGiacomo Vitturi, Luca Piccoli, Andrea Spini, et al.
Pharmaceutical Medicine|August 20, 2026
Empowering Medical Affairs Professionals in Their Critical Role in Integrated Evidence Generation PlanningJudith Nelissen, Angela Williams, Cerise James, et al.
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