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Pharmaceutical Medicine|July 3, 2022
Global Landscape of Benefit-Risk Considerations for Medicinal Products: Current State and Future DirectionsMax Waschbusch, Lisa Rodriguez, Andreas Brueckner, et al.Pharmaceutical Medicine|July 5, 2022
A Structured Methodology to Assess Safety Signal Strength and Inform Causality AssessmentTim Sullivan, Magnus Nord, Doug Domalik, et al.Pharmaceutical Medicine|October 28, 2020
Plain Language Summaries of Clinical Trial Results: A Preliminary Study to Assess Availability of Easy-to-Understand Summaries and Approaches to Improving Public EngagementMichael Penlington, Harold Silverman, Ajithkumar Vasudevan, et al.Pharmaceutical Medicine|September 15, 2020
Electronic Reporting Systems in Pharmacovigilance: The Implementation of VigiFlow in BrazilMarcelo Vogler, Heloísa Ricci Conesa, Karla de Araújo Ferreira, et al.Pharmaceutical Medicine|June 20, 2022
An Industry Survey on Managing the Pharmacovigilance System Master File in a Global Environment: The Need for a Pragmatic ApproachClare Lavery, Joanne Emmott, Sabine Jeck-Thole, et al.Pharmaceutical Medicine|September 4, 2018
Excipients in Neonatal Medicinal Products: Never Prescribed, Commonly AdministeredKristine Svinning Valeur, Helle Holst, Karel AllegaertPharmaceutical Medicine|February 4, 2021
The conect4children (c4c) Consortium: Potential for Improving European Clinical Research into Medicines for ChildrenMark A Turner, Heidrun Hildebrand, Ricardo M Fernandes, et al.Pharmaceutical Medicine|April 14, 2025
Importance of Health Economics and Outcomes Research in the Product LifecycleAmit DangPharmaceutical Medicine|April 16, 2013
Will the EU Clinical Trials Regulation Support the Innovative Industry in Bringing New Medicines Faster to Patients?Sabine Atzor, Surendra Gokhale, Michael DohertyPharmaceutical Medicine|December 29, 2009
Electronic Diaries: Appraisal and Current StatusJoan E BroderickPageof 31