Altmetric Data is Now Available for ClinicalTrials.gov Study Records – Altmetric
Downloading Content for Analysis - ClinicalTrials.gov
MIT Guide to PHS Human Subjects and Clinical Trial Information Form and Study Record for KC S2S and Workspace
MIT Guide to PHS Human Subjects and Clinical Trial Information Form and Study Record for KC S2S and Workspace
Clinical Trials - ScienceDirect
Study Record - Section 1 Basic Information
ClinicalTrials.gov Registration and Results Guide
Clinical trial design during and beyond the pandemic: the I-SPY COVID trial | Nature Medicine
How to Find Results of Studies - ClinicalTrials.gov
Building an open database of information on all clinical trials
Efficacy and safety of hydroxychloroquine as pre-and post-exposure prophylaxis and treatment of COVID-19: A systematic review and meta-analysis of blinded, placebo-controlled, randomized clinical trials. - The Lancet Regional Health – Americas
Protocol Registration and Results System (PRS) Overview
Incorporating Site-less Clinical Trials Into Drug Development: A Framework for Action - Clinical Therapeutics
Storage and Archiving of Research Documents SOP 6
Research Instructions for NIH and Other PHS Agencies
Information on blinding in registered records of clinical trials | Trials | Full Text
MIT Guide to PHS Human Subjects and Clinical Trial Information Form and Study Record for KC S2S and Workspace
QUICK GUIDE PHS HUMAN SUBJECTS & CLINICAL TRIALS INFORMATION NIH HUMAN SUBJECT STUDY RECORD ATTACHMENT
Celebrating 20 Years of ClinicalTrials.gov and Looking to the Future – NLM Musings from the Mezzanine
CT08: Clinical Trial Monitoring: Study Monitoring, Documentation and Closure | Zenosis – Learning for Life
Current use and costs of electronic health records for clinical trial research: a descriptive study | CMAJ Open
All about Clinical Trial Data Management | Smartsheet
Study Record - Section 6 Clinical Milestone Plan
Clinical Research Coordinator (CRC) | MindMeister Mind Map
Using ClinicalTrials.gov as a Resource
Using the Cochrane Central Register of Controlled Trials to identify clinical trial registration is insufficient: a cross-sectional study | BMC Medical Research Methodology | Full Text
Comparison between efficacy/safety and pragmatic trials. AE, adverse... | Download Scientific Diagram
