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Therapeutic Innovation & Regulatory Science|May 17, 2023
Digital Tools-Regulatory Considerations for Application in Clinical TrialsLian Gelis, Isabelle Stoeckert, Hans-Peter PodhaiskyThe Patient|January 28, 2025
What Next for the Science of Patient Preference? Interoperability, Standardization, and TransferabilityKevin Marsh, Juan Marcos Gonzalez Sepulveda, Conny Berlin, et al.Frontiers in Pharmacology|September 4, 2023
How can patient preferences be used and communicated in the regulatory evaluation of medicinal products? Findings and recommendations from IMI PREFER and call to actionRosanne Janssens, Liese Barbier, Mireille Muller, et al.Pharmacoepidemiology and Drug Safety|May 14, 2014
Balancing benefit and risk of medicines: a systematic review and classification of available methodologiesShahrul Mt-Isa, Christine E Hallgreen, Nan Wang, et al.Pharmacoepidemiology and Drug Safety|July 22, 2014
Benefit-risk assessment in a post-market setting: a case study integrating real-life experience into benefit-risk methodologyChristine E Hallgreen, Hendrika A van den Ham, Shahrul Mt-Isa, et al.Pageof 1