Study Reporting Compliance Over Time - Years.

<div><p>Introduction</p><p>Accurate and timely reporting of scientific knowledge is crucial to clinical research ethics. ClinicalTrials.gov allows researchers to register trials and report results to the public and scientific community. Despite FDA reporting mandates, complia...

Full description

Saved in:

Bibliographic Details
Main Author:	Nicholas Kendall (21376780) (author)
Other Authors:	Julian S. Rechberger (21376783) (author), Abdelrahman M. Hamouda (18180083) (author), Mark Cwajna (21376786) (author), Sherief Ghozy (6742202) (author), Kogulavadanan Arumaithurai (8397918) (author), David F. Kallmes (4744215) (author)
Published:	2025
Subjects:	Medicine Biotechnology Immunology Developmental Biology Cancer Science Policy Infectious Diseases previously published algorithm factors significantly associated create targeted incentives available trial dates 46 &# 8211 37 &# 8211 04 &# 8211 lower reporting rates factors influenced reporting gov likely mandated gov allows researchers xlink "> accurate reporting mandates remains reported results within identify factors related identified 255 gbm clinical research ethics xlink "> reporting mandates year reporting timely reporting related trials study design study aimed scientific knowledge scientific community register trials quadruple masking month deadline major issue increase transparency identify studies five years especially important biological interventions benefiting patients aggressive nature advancing research 2 trials 014 ),
Tags:	Add Tag No Tags, Be the first to tag this record!

Be the first to leave a comment!

Study Reporting Compliance Over Time - Years.

Similar Items