Selective reporting in trials of high risk cardiovascular devices: cross sectional comparison between premarket approval summaries and published reports

類似資料

• Assessment of Clinical Trial Evidence for High-Risk Cardiovascular Devices Approved Under the Food and Drug Administration Priority Review Program
  著者:: Jones, L. Camille, 等
  出版事項: (2018)
• Characteristics of Clinical Studies Used for US Food and Drug Administration Approval of High-Risk Medical Device Supplements
  著者:: Zheng, Sarah Y., 等
  出版事項: (2017)
• Comparison of Priority vs Standard US Food and Drug Administration Premarket Approval Review for High-Risk Medical Devices
  著者:: Ong, Caroline, 等
  出版事項: (2020)
• Medical Device Regulation: Time to Improve Performance
  著者:: Dhruva, Sanket S., 等
  出版事項: (2012)
• Inclusion of Demographic-Specific Information in Studies Supporting US Food & Drug Administration Approval of High-Risk Medical Devices
  著者:: Dhruva, Sanket S., 等
  出版事項: (2017)