User Guides
These ECOS User Guides are intended to assist and guide the NHG & NUHS Research Communities, our Partner Institutions and Industry Partners when they are using the ECOS system.
You can also use the Search Function (found on the page's top-right corner) to locate the information you need.
Do check back regularly for updates and new additions.
General ECOS Functionality & Overview
Creating New User Accounts & General Overview
This guidebook shows how new Public Healthcare Institutions (PHI) Users can login and create their ECOS User Accounts. It also provides information on the NHG Minimum Training requirements and orientates Users to the ECOS interface and layout. (Last updated: 7 May 2024)
Submitting Minimum Training Certification
This guidebook will show ECOS Users how to access the Minimum Training Module to upload their training certificates into their User Profile. (Last updated: 7 May 2024)
Submitting Financial Conflict of Interest (FCOI) Declarations
This guidebook introduces the Financial Conflict of Interest (FCOI) Module and shows how Users can submit their FCOI Declarations as well as responding to queries from the FCOI Secretariat. (Last updated: 7 May 2024)
IRB Ethics Submissions
Overview of IRB Ethics Submissions
This Guidebook provides an overview and user-orientation to the Institutional Review Board (IRB) Module. It explains the IRB submission process for new Study Submissions and for the various reporting Forms for approved active studies. (Last updated 9 May 2024)
How to prepare for IRB Ethics Submissions
This quick guide explains how to successfully prepare for an IRB submission, in particular, by looking at the User Profiles, Minimum Training and FCOI Declaration requirements. (Last updated: 13 August 2024)
IRB Ethics Application Form - List of Sections & Questions
This guidebook provides a complete listing of all the Sections and Questions in the IRB Application Form for reference so that researchers can draft their IRB Application Form. (Last updated: 1 March 2024)
Managing Your Research Activity
Using the Clinical Research Management System (CRMS) to manage research projects and activities
This guidebook introduces the new ECOS Clinical Research Management System (CRMS) module which is a useful clinical research management tool at the Site, Study and Institutional level.
Researchers can use the CRMS module to record, track and manage their respective clinical research projects and activities, including managing the User Authorization List which controls user access to CRMS, IRB and other modules for Study Team Roles (ie: Study Administrators, Collaborators, Study Sponsor, etc). (Last updated: 21 May 2024)
How to Add New Study Team Members to your Study on ECOS
This quick guide explains how a Principal Investigator (PI) can add and endorse/approve new Study Team Members via the Study’s User Authorization List (UAL) in the ECOS Clinical Research Management System (CRMS) module (Last updated: 7 June 2024)
How to Add and Endorse New Study Team members in ECOS
This quick guide explains how the current Team Members can add new Team Members via the Study’s User Authorization List (UAL) in the ECOS Clinical Research Management System (CRMS) module. (Last updated 24 June 2024)
How to manage Multi-Site Studies in ECOS
This quick guide explains how researchers can set up and manage multiple Study Sites in ECOS by using the ECOS Clinical Research Management System (CRMS) module (Last updated: 22 July 2024)
How to Access Different Modules on ECOS
This quick guide explains how researchers can access different modules on ECOS. (Last updated: 18 Sep 2024)
Responding to the NHG Research Institution for Deviation/ Non-Compliance & Serious Adverse Events from HBR Studies
How to manage DNC & SAE from HBR Studies
This guidebook provides Users with a step-by-step guidance to help users navigate the module. (Last updated 1 August 2024)
Standing Database (SDB) Submissions
SDB User Module Guide
A. For Users - This guide provides Users with step-by-step guidance on the submission of an SDB application and navigation of the module.
B. For Endorsers (ROC/DR/IR) – This guide provides endorsers with step-by-step guidance on the endorsement of an SDB application and navigation of the module.
These guides are only applicable to NHG and NUHS users (Last update on 25 October 2024).
For Users – Download here.
For Endorsers (RDOC/DR/IR) – Download here.
SDB Forms Guidebook
This guidebook provides a complete listing of all the Questions in the SDB Application Form, Non-Compliance Report (NCR) Form and Status Report Form (SRF). (Last updated 10 October 2024)
For ECOS Institution & Department Representatives
How Inst & Dept Reps can locate and complete their Endorsement Tasks
This guidebook is intended for ECOS Users who are appointed as Institution or Department Representatives (IR & DR). It provides information and a step-by-step guide on the IR & DR Ethics Submission Endorsement process. (Last updated 7 May 2024)
Research Quality Programmes
How to complete the PISAF & SCC
This guidebook contains step-by-step guidance for PIs/ Site-PIs/ Co-Investigators and Study Team Members to navigate the module interface and to complete the submission process for the PISAF/ SCC on ECOS Compliance module.
Only selected PIs will be informed to complete the PISAF/SCC.
(Last updated: 27 Sep 2024)