NIH Extramural Research Records Schedule
Guidance for Research Data and Materials Security
ETCTN Regulatory Processing Information Sheet
Clinical Research Study Investigator's Toolbox | National Institute on Aging
PHS Human Subjects and Clinical Trials Information Form Walk-through - YouTube
Free Clinical Trial Templates | Smartsheet
Free Clinical Trial Templates | Smartsheet
NIA-Funded Active Alzheimer's and Related Dementias Clinical Trials and Studies | National Institute on Aging
4 Questions For Researchers and Institutions Involved In Human Subjects Research – NIH Extramural Nexus
Clinical research process | Research Support
Records Management Schedule and Storage
Guidance Document: Part C, Division 5 of the Food and Drug Regulations “Drugs for Clinical Trials Involving Human Subjects” (GUI-0100) - Canada.ca
NIH Records Management Program
Transition from Inclusion Management System to New Human Subjects System (HSS) as of June 9, 2018 Purpose
Essential Documents & Master Files | Compass
Archiving
Digitizing clinical trials | npj Digital Medicine
Frequently Asked Questions - ClinicalTrials.gov
NIH Data Management and Sharing Policy (2023) | Data Cooperative
Essential Documents & Master Files | Compass
Investigational Products: IP Management and Accountability
Ten simple rules for maximizing the recommendations of the NIH data management and sharing plan | PLOS Computational Biology
NIH Records Management Program
Celebrating 20 Years of ClinicalTrials.gov and Looking to the Future – NLM Musings from the Mezzanine
01 Introduction.docx
