Literature DB >> 34028509

Evaluation of Compliance With Legal Requirements Under the FDA Amendments Act of 2007 for Timely Registration of Clinical Trials, Data Verification, Delayed Reporting, and Trial Document Submission.

Nicholas J DeVito1, Ben Goldacre1.   

Abstract

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Year:  2021        PMID: 34028509      PMCID: PMC8145152          DOI: 10.1001/jamainternmed.2021.2036

Source DB:  PubMed          Journal:  JAMA Intern Med        ISSN: 2168-6106            Impact factor:   44.409


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  2 in total

1.  Inadequate reporting quality of registered genome editing trials: an observational study.

Authors:  Diana Jurić; Michael Zlatin; Ana Marušić
Journal:  BMC Med Res Methodol       Date:  2022-05-02       Impact factor: 4.612

2.  Trends in patient-reported outcome use in early phase dose-finding oncology trials - an analysis of ClinicalTrials.gov.

Authors:  Julia Lai-Kwon; Zhulin Yin; Anna Minchom; Christina Yap
Journal:  Cancer Med       Date:  2021-10-22       Impact factor: 4.452

  2 in total

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