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Pharmaceutical Medicine|December 16, 2025
Publicly Available Clinical Trial Safety Data: Review and a Call for Standardization and Improved Reporting PracticesBarbara A Hendrickson, Cynthia McShea, Tarek A Hammad, et al.Pharmaceutical Medicine|December 1, 2025
Considerations for Biosimilar Adoption in Pediatrics: A Scoping ReviewElaine Lau, Alicia Koo, Han Byul Kang, et al.Pharmaceutical Medicine|December 9, 2023
"Regulatory Sandboxes" Could Solve the Regulatory Problems Encountered in Europe and Arising from Innovation in Biological Medicinal ProductsMathieu GuerriaudPharmaceutical Medicine|December 22, 2023
The Importance of Assessing Drug Exposure and Medication Adherence in Evaluating Investigational Medications: Ensuring Validity and Reliability of Clinical Trial ResultsBernard Vrijens, Antoine Pironet, Eric ToussetPharmaceutical Medicine|November 29, 2023
A Review of the Current FDA-Approved Antibody-Drug Conjugates: Landmark Clinical Trials and IndicationsMeghana Kesireddy, Srikanth Reddy Kothapalli, Sai Giridhar Gundepalli, et al.Pharmaceutical Medicine|February 1, 2024
Meaningful Within-Patient Change in Subjective Total Sleep Time in Patients with Insomnia Disorder: An Analysis of the Sleep Diary Questionnaire Using Data from Open-Label and Phase III Clinical TrialsAndrea Phillips-Beyer, Ariane K Kawata, Leah Kleinman, et al.Pharmaceutical Medicine|March 31, 2024
Authorized or Off-Label Use? A Structured Analysis of Summaries of Product Characteristics with Regard to Authorization in PediatricsMarkus Herzig, Simone Eisenhofer, Meike Ruschkowski, et al.Pharmaceutical Medicine|June 27, 2023
A Survey of Industry Perceptions of Facilitated Regulatory Pathways in Drug Development in AustraliaAlina Yoffe, Johnson Liu, Greg Smith, et al.Pharmaceutical Medicine|February 26, 2026
The Combat Against Antimicrobial Resistance: An Overview of EU Recent Health Policies and Drug Regulations Promoting the Development of New AntimicrobialsLena Daher, Ingrid Vilimelis-PiulatsPageof 31