04949nam 2200625 450 991078744080332120230803212547.00-309-31003-20-309-31001-6(CKB)3710000000336166(EBL)3379407(SSID)ssj0001467018(PQKBManifestationID)11892276(PQKBTitleCode)TC0001467018(PQKBWorkID)11504063(PQKB)11321513(MiAaPQ)EBC3379407(Au-PeEL)EBL3379407(CaPaEBR)ebr11003355(OCoLC)904080937(EXLCZ)99371000000033616620150121h20142014 uy 0engurcnu||||||||txtccrCharacterizing and communicating uncertainty in the assessment of benefits and risks of pharmaceutical products workshop summary /Denise Caruso, Rebecca A. English, Anne B. ClaiborneWashington, District of Columbia :The National Academies Press,2014.©20141 online resource (150 p.)Description based upon print version of record.0-309-31000-8 Includes bibliographical references.""Front Matter""; ""Reviewers""; ""Contents""; ""Boxes, Figures, and Table""; ""Acronyms""; ""1 Introduction""; ""2 Identifying and Characterizing Uncertainty""; ""3 The Regulators Challenge""; ""4 Basic Methodologies and Applications for Understanding and Evaluating Uncertainty""; ""5 Communicating Uncertainty""; ""6 Final Reflections on Ways to Characterize and Communicate Uncertainty""; ""References""; ""Appendix A: Workshop Agenda""; ""Appendix B: FDA Case Studies""; ""Appendix C: Bibliography""; ""Appendix D: Participant Biographies"""Despite the extensive body of evidence that informs regulatory decisions on pharmaceutical products, significant uncertainties persist, including the underlying variability in human biology, factors associated with the chemistry of a drug, and limitations in the research and clinical trial process itself that might limit the generalizability of results. As a result, regulatory reviewers are consistently required to draw conclusions about a drug's safety and efficacy from imperfect data. Efforts are underway within the drug development community to enhance the evaluation and communication of the benefits and risks associated with pharmaceutical products, aimed at increasing the predictability, transparency, and efficiency of pharmaceutical regulatory decision making. Effectively communicating regulatory decisions necessarily includes explanation of the impact of uncertainty on decision making. On February 12 and May 12, 2014, the Institute of Medicine's Forum on Drug Discovery, Development, and Translation held public workshops to advance the development of more systematic and structured approaches to characterize and communicate the sources of uncertainty in the assessment of benefits and risks, and to consider their implications for pharmaceutical regulatory decisions. Workshop presentations and discussions on February 12 were convened to explore the science of identifying and characterizing uncertainty in scientific evidence and approaches to translate uncertainties into decisions that reflect the values of stakeholders. The May 12 workshop presentations and discussions explored tools and approaches to communicating about scientific uncertainties to a range of stakeholders in the drug development process. Characterizing and Communicating Uncertainty in the Assessment of Benefits and Risks of Pharmaceutical Products summarizes the presentation and discussion of both events. This report explores potential analytical and communication approaches and identifies key considerations on their development, evaluation, and incorporation into pharmaceutical benefit- risk assessment throughout the entire drug development lifecycle"--Publisher's description.Risk assessmentCongressesCommunicationCongressesRisk assessmentCommunication363.1Caruso Denise1545137English Rebecca A.Claiborne Anne B.Board on Health Sciences Policy.Institute of Medicine (U.S.).Forum on Drug Discovery, Development, and Translation.Institute of Medicine (U.S.)Characterizing and Communicating Uncertainty in the Assessment of Benefits and Risks of Pharmaceutical Products (Workshop)(2014 :White Oak, Md.),MiAaPQMiAaPQMiAaPQBOOK9910787440803321Characterizing and communicating uncertainty in the assessment of benefits and risks of pharmaceutical products3799892UNINA