日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Using Historical Data to Support Approval of Drug Products for Ophthalmia Neonatorum: Innovative Approach Toward Evidence-Based Medicine

利用历史数据支持新生儿眼炎药物的审批:迈向循证医学的创新方法

Sun, Haihao; Temeck, Jean W; McCune, Susan K; Chambers, Wiley A

Common Commentary on Paediatric Oncology Drug Development Published: Another Step in Optimising Global Regulatory Coordination of Paediatric Development Plans

关于儿科肿瘤药物研发的共同评论已发布:优化全球儿科研发计划监管协调的又一举措

Karres, Dominik; Reaman, Gregory; Ligas, Franca; Lesa, Giovanni; McCune, Susan; Malli, Suzanne; Bax, Ralph; Temeck, Jean

Duration of Pediatric Clinical Trials Submitted to the US Food and Drug Administration

提交给美国食品药品监督管理局的儿科临床试验持续时间

Zimmerman, Kanecia O; Smith, P Brian; McMahon, Ann W; Temeck, Jean; Avant, Debbie; Murphy, Dianne; McCune, Susan

Pediatric Medicine Development: An Overview and Comparison of Regulatory Processes in the European Union and United States

儿科药物研发:欧盟与美国监管流程概述及比较

Penkov, Dobromir; Tomasi, Paolo; Eichler, Irmgard; Murphy, Dianne; Yao, Lynne P; Temeck, Jean

Extrapolation of Efficacy in Pediatric Drug Development and Evidence-based Medicine: Progress and Lessons Learned

儿科药物研发和循证医学中的疗效外推:进展与经验教训

Sun, Haihao; Temeck, Jean W; Chambers, Wiley; Perkins, Ginger; Bonnel, Renan; Murphy, Dianne