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Improving FDA postmarket adverse event reporting for medical devices

Authors

  • Susmitha Wunnava Harvard-MIT Center for Regulatory Science, Harvard Medical School, Boston, Massachusetts, USAComputational Health Informatics Program, Boston Children's Hospital, Boston, Massachusetts, USA PubMed articlesGoogle scholar articles
  • Timothy A Miller Computational Health Informatics Program, Boston Children's Hospital, Boston, Massachusetts, USADepartment of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA PubMed articlesGoogle scholar articles
  • Florence T Bourgeois Computational Health Informatics Program, Boston Children's Hospital, Boston, Massachusetts, USADepartment of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Florence T Bourgeois, Boston Children's Hospital, Boston, MA 02115, USA; Florence.Bourgeois{at}childrens.harvard.edu
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Citation

Wunnava S, Miller TA, Bourgeois FT
Improving FDA postmarket adverse event reporting for medical devices

Publication history

  • Accepted January 21, 2022
  • First published February 17, 2022.

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