يعرض 1 - 10 نتائج من 71 نتيجة بحث عن '"expedited review"', وقت الاستعلام: 0.91s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Pediatric polysomnography-flagging etiologies and impact on the clinical timeline

    المؤلفون: Seema Rani, John Schanz, Kapil Chauhan, August Kolb, Victoria Gatta, Abigail Strang, Aaron C. Chidekel

    المصدر: Frontiers in Sleep, Vol 2 (2024)

    مصطلحات موضوعية: polysomnography, abnormal sleep studies, expedited review, pediatrics, obstructive sleep apnea, Medicine

    وصف الملف: electronic resource

    Relation: https://www.frontiersin.org/articles/10.3389/frsle.2023.1302509/full; https://doaj.org/toc/2813-2890

    URL الوصول: https://doaj.org/article/f8c7b5aedbbb4b128fd6462b678f47a7

    Full Text Finder
    أضف إلى المفضلة
  2. 2
    دورية أكاديمية
    Modeling Approaches to Reimagine Stability (MARS) for Enabling Earlier Access to Critical Drugs for Patients with Unmet Medical Needs

    المؤلفون: Furness, M. ScottAff1, IDs12249022024980_cor1, Cai, Hong, Chandramouli, Sithamalli, Chelliah, Mariappan, Chen, Xiao Hong, Ghosh, Debasis, Liu, Shaobo, McLamore, Sherita, Randad, Ramnarayan, Shen, Meiyu

    المصدر: AAPS PharmSciTech: An Official Journal of the American Association of Pharmaceutical Scientists. 24(1)

    Find this article in full text from Springer Verlag. Full Text Finder
    أضف إلى المفضلة
  3. 3
    دورية أكاديمية
    Maximizing Regulatory Review Efficiency: The Evolution of the FDA OCE RTOR Pilot

    المؤلفون: Gao, Ya GraceAff1, Aff2, IDs4344102100371z_cor1, Roberts, Samantha, Guy, Allison

    المصدر: Therapeutic Innovation & Regulatory Science. 56(2):212-219

    Find this article in full text from Springer Verlag. Full Text Finder
    أضف إلى المفضلة
  4. 4
    دورية أكاديمية
    Registration pathways to accelerate regulatory assessment of innovative medicines in Latin America

    المؤلفون: Padua, AnaAff1, Partika, Livia, Bonamici, Denise, Rahal Cabello, Juliana, Kohiyama, Cristiane, Spinardi, Paula, Castro, Anabelle, Rolim, Alessandra, Souto, Francisco

    المصدر: Journal of Public Health Policy. 41(4):481-495

    Find this article in full text from Springer Verlag. Find this article in full text from ProQuest Full Text Finder
    أضف إلى المفضلة
  5. 5
    كتاب إلكتروني
    Institutional Review Board (IRB)

    المؤلفون: East, CaraAff2

    المساهمون: East, CaraAff1

    المصدر: Developing a Successful Clinical Research Program. :69-76

    أضف إلى المفضلة
  6. 6
    دورية أكاديمية
    From the Valley of Death to the Crossroads of Opportunity: A Discussion of Evolving Benefit/Risk Evaluation Standards

    المؤلفون: Pitts, Peter J.Aff1, Aff2, Brady, Patrick

    المصدر: Therapeutic Innovation & Regulatory Science. 52(5):531-536

    Find this article in full text from Springer Verlag. Full Text Finder
    أضف إلى المفضلة
  7. 7
    دورية أكاديمية
    Effects of Human Subjects Requirements on Classroom Research: Multidisciplinary Evidence

    المؤلفون: Lopus, Jane S., Grimes, Paul W., Becker, William E., Pearson, Rodney A.

    المصدر: Journal of Empirical Research on Human Research Ethics: An International Journal, 2007 Sep . 2(3), 69-78.

    URL الوصول: https://www.jstor.org/stable/10.1525/jer.2007.2.3.69

    Find this article in full text from ProQuest View record at SAGE Research Methods Full Text Finder
    أضف إلى المفضلة
  8. 8
    دورية أكاديمية
    The Potential Benefit of Expedited Development and Approval Programs in Precision Medicine

    المؤلفون: Ariel Kantor, Susanne B. Haga

    المصدر: Journal of Personalized Medicine, Vol 11, Iss 1, p 45 (2021)

    مصطلحات موضوعية: regulation, drugs, precision medicine, expedited review, orphan drugs, Medicine

    وصف الملف: electronic resource

    Relation: https://www.mdpi.com/2075-4426/11/1/45; https://doaj.org/toc/2075-4426

    URL الوصول: https://doaj.org/article/fe8f62f1f525425ca770fbfae4d72d09

    Find this article in full text from ProQuest Full Text Finder
    أضف إلى المفضلة
  9. 9
    Maximizing Regulatory Review Efficiency: The Evolution of the FDA OCE RTOR Pilot

    المؤلفون: Ya Grace Gao, Samantha Roberts, Allison Guy

    المصدر: Therapeutic Innovation & Regulatory Science

    مصطلحات موضوعية: Oncology drug review, FDA OCE pilot programs, Real-time oncology review, United States Food and Drug Administration, Public Health, Environmental and Occupational Health, Analytical Report, US food and drug administration, United States, Expedited review program, Pharmaceutical Preparations, Research Design, Pharmacology (medical), Drug Approval, Pharmacology, Toxicology and Pharmaceutics (miscellaneous), Oncology center of excellence

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b83501b1b0f63d719ca39c1369f9ed67
    https://doi.org/10.1007/s43441-021-00371-z

    Find this article in full text from Springer Verlag.
    أضف إلى المفضلة
  10. 10
    دورية أكاديمية

    لا يتم عرض هذه النتيجة على الضيوف.

    View record in Scopus
    أضف إلى المفضلة
أدوات البحث: أحصل على تغذية RSS – أرسل هذا البحث بالبريد الإلكتروني – حفظ البحث – جدول التنبيهات: لا شيء