(Izdošanas datums: 03-Jul-2024, PDF+DRM, Izdevniecība: Taylor & Francis Ltd, ISBN-13: 9781040042069)
The management of clinical data, from its collection during a trial to its extraction for analysis, has become critical in preparing a regulatory submission and obtaining approval to market a treatment. Groundbreaking on its initial publication nearl...Lasīt vairāk
(Izdošanas datums: 03-Jul-2024, EPUB+DRM, Izdevniecība: Taylor & Francis Ltd, ISBN-13: 9781040042113)
The management of clinical data, from its collection during a trial to its extraction for analysis, has become critical in preparing a regulatory submission and obtaining approval to market a treatment. Groundbreaking on its initial publication nearl...Lasīt vairāk
This book considers the intellectual property protection of clinical test data that has been submitted to governments, in particular through test data exclusivity rights. It focuses on how these intellectual property rights first emerged in the early...Lasīt vairāk
This book considers the intellectual property protection of clinical test data that has been submitted to governments, in particular through test data exclusivity rights. It focuses on how these intellectual property rights first emerged in the early...Lasīt vairāk
National Academies of Sciences, Engineering, and Medicine, Health and Medicine Division, Board on Health Care Services, Board on Health Sciences Policy, Roundtable on Genomics and Precision Health, National Cancer Policy Fo
(Izdošanas datums: 20-Oct-2020, EPUB+DRM, Izdevniecība: National Academies Press, ISBN-13: 9780309679183)
On November 18 and 19, 2019, the National Academies of Sciences, Engineering, and Medicine hosted a public workshop in Washington, DC, titled Sharing Clinical Trial Data: Challenges and a Way Forward. The workshop followed the release of the 2015 Ins...Lasīt vairāk
Institute of Medicine, Board on Health Sciences Policy, Committee on Strategies for Responsible Sharing of Clinical Trial Data
(Izdošanas datums: 22-Jan-2014, EPUB+DRM, Izdevniecība: National Academies Press, ISBN-13: 9780309297820)
Sharing data generated through the conduct of clinical trials offers the promise of placing evidence about the safety and efficacy of therapies and clinical interventions on a firmer basis and enhancing the benefits of clinical trials. Ultimately, su...Lasīt vairāk
Institute of Medicine, Board on Health Sciences Policy, Committee on Strategies for Responsible Sharing of Clinical Trial Data
(Izdošanas datums: 22-Jan-2014, PDF+DRM, Izdevniecība: National Academies Press, ISBN-13: 9780309297806)
Sharing data generated through the conduct of clinical trials offers the promise of placing evidence about the safety and efficacy of therapies and clinical interventions on a firmer basis and enhancing the benefits of clinical trials. Ultimately, su...Lasīt vairāk
(Izdošanas datums: 15-Jun-2010, EPUB+DRM, Izdevniecība: John Wiley & Sons Inc, ISBN-13: 9780470438565)
ExpDesign Studio facilitates more efficient clinical trial design This book introduces pharmaceutical statisticians, scientists, researchers, and others to ExpDesign Studio software for classical and adaptive designs of clinical trials. It includes...Lasīt vairāk
Recent progress in high-throughput screening, combinatorial chemistry and molecular biology has radically changed the approach to drug discovery in the pharmaceutical industry. New challenges in synthesis result in new analytical methods. At present,...Lasīt vairāk
(Izdošanas datums: 02-Jul-2008, PDF+DRM, Izdevniecība: John Wiley & Sons Inc, ISBN-13: 9780470369975)
ExpDesign Studio facilitates more efficient clinical trial design This book introduces pharmaceutical statisticians, scientists, researchers, and others to ExpDesign Studio software for classical and adaptive designs of clinical trials. It includes...Lasīt vairāk
