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
Investigator Community - CTTI
Safety reporting forms for clinical research projects - Tools & Resources
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
CT14: Clinical Trial Safety Reporting Requirements in the EU and USA | Zenosis – Learning for Life
Process of reporting serious adverse events (SAE) during a regulatory... | Download Scientific Diagram
Reporting guidelines for clinical trial reports for interventions involving artificial intelligence: the CONSORT-AI extension | Nature Medicine
Steps for a Successful Clinical Trial Management System
Months and Severity Score (MOSES) in a Phase III trial (PARCER): A new comprehensive method for reporting adverse events in oncology clinical trials - eClinicalMedicine
Global Healthcare Brand Improves Safety Reporting in Clinical Trials Leveraging Pharmacovigilance Analytics| Quantzig | Business Wire
Safety reporting in clinical research: choosing the right workflow
Reporting of adverse events at ClinicalTrials.gov and in published... | Download Table
Clinical Trials: A Practical Guide to Design, Analysis and Reporting: Wang, Duolao: 9781901346725: Amazon.com: Books
COVID-19 Guidance: Reporting on Clinical Trials - Information Saves Lives | Internews
SAFETY REPORTING IN CLINICAL TRIALS | Clinical trials, Clinic, Clinical research