After years of lax oversight, the NIH is starting to contact institutions about unreported clinical trial results - STAT
Reporting of adverse events at ClinicalTrials.gov and in published... | Download Table
Compliance with legal requirement to report clinical trial results on ClinicalTrials.gov: a cohort study - The Lancet
How to Report Clinical Trial Results | Research Ethics & Compliance
PPT - Safety Reporting IN Clinical Trials PowerPoint Presentation - ID:3196235
CRO - Next Stage Clinical Research
Safety reporting in clinical research: choosing the right workflow
Months and Severity Score (MOSES) in a Phase III trial (PARCER): A new comprehensive method for reporting adverse events in oncology clinical trials - eClinicalMedicine
Steps for a Successful Clinical Trial Management System
Safety reporting forms for clinical research projects - Tools & Resources
Clinical Trials Adverse Event Reporting Guide, 2022 Edition | CenterWatch
Under-reporting of harm in clinical trials - The Lancet Oncology
AllTrials – Study finds poor clinical trial reporting from leading academic centres
SAFETY REPORTING IN CLINICAL TRIALS | Clinical trials, Clinic, Clinical research
COVID-19 Guidance: Reporting on Clinical Trials - Information Saves Lives | Internews
Safety reporting forms for clinical research projects - Tools & Resources
Racial and ethnic enrollment disparities and demographic reporting requirements in acute leukemia clinical trials | Sustainable Development Goals - Resource Centre
CT14: Clinical Trial Safety Reporting Requirements in the EU and USA | Zenosis – Learning for Life
Global Healthcare Brand Improves Safety Reporting in Clinical Trials Leveraging Pharmacovigilance Analytics| Quantzig | Business Wire
Clinical Trials: A Practical Guide to Design, Analysis and Reporting: Wang, Duolao: 9781901346725: Amazon.com: Books
NIH Clinical Trials Reporting Compliance: A Shared Commitment – NIH Extramural Nexus
Improving outcome reporting in clinical trial reports and protocols: study protocol for the Instrument for reporting Planned Endpoints in Clinical Trials (InsPECT) | Trials | Full Text
Reporting guidelines for clinical trial reports for interventions involving artificial intelligence: the CONSORT-AI extension | Nature Medicine
SLHD RPA - Research Ethics and Governance Office - Safety Reporting
Comparison of serious adverse events posted at ClinicalTrials.gov and published in corresponding journal articles – The Publication Plan for everyone interested in medical writing, the development of medical publications, and publication planning
Investigator Community - CTTI
EU Explains Safety Reporting Under New Clinical Trial Regs :: Pink Sheet
