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PDF] Effective authoring of clinical study reports: A companion guide | Semantic Scholar
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Under-reporting of harm in clinical trials - The Lancet Oncology
Compliance with legal requirement to report clinical trial results on ClinicalTrials.gov: a cohort study - The Lancet
For first time, the FDA warns a researcher for failing to report trial results
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Clinical study reports of randomised controlled trials: an exploratory review of previously confidential industry reports | BMJ Open
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Completeness of Reporting of Patient-Relevant Clinical Trial Outcomes: Comparison of Unpublished Clinical Study Reports with Publicly Available Data | PLOS Medicine
Sponsors of clinical trials may report data late or never | Spectrum | Autism Research News
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Completeness of Reporting of Patient-Relevant Clinical Trial Outcomes: Comparison of Unpublished Clinical Study Reports with Publicly Available Data | PLOS Medicine
Will clinical trial data disclosure reduce incentives to develop new uses of drugs? | Nature Biotechnology
Compliance with Results Reporting at ClinicalTrials.gov | NEJM
Safety reporting forms for clinical research projects - Tools & Resources
Guidelines for clinical trial protocols for interventions involving artificial intelligence: the SPIRIT-AI extension - The Lancet Digital Health
More than half of EU clinical trials do not comply with rules
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2022 State of Clinical Trial Operations Technology Report - Florence
Digital Transformation In The Critical Path Of The Clinical Trial | An Overview - Part 1
Appendix F Illustrative Data Fields for the Results Summary | Developing a National Registry of Pharmacologic and Biologic Clinical Trials: Workshop Report | The National Academies Press
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