R&D Permissions Process (multicentre)

Slides:



Advertisements
Similar presentations
Document #06-4G Enrollment Process (via Uniform Electronic Transaction) Customer Supplier Distribution Company Customer authorizes Enrollment Supplier.
Advertisements

1 Drop Submitted by Supplier Customer Supplier Distribution Company Supplier sends Drop Request to Distribution Company (??) Distribution Company receives.
The HRPP FYI Process and the UPIRSO/SAE Review Sheet An IRB Infoshort February 2014.
Electronic-only submission of FP7 financial statements (forms C) NEXT.
Attendance and Truancy Packet Procedures Las Cruces Public Schools Attendance and Student Services.
ProTECT III Regulatory & Project Management. Project Spoke Table This is where information about your Spokes is maintained This is where information about.
USF Research Integrity & Compliance eIRB Comprehensive Training 10/07/2014.
The Head Start Key Indicator Screener This information is considered to be privileged information per Exemption (b)(4) under FOIA and not releasable per.
Laura Noll Research Compliance Manager Radford University.
NHS Research Scotland -Overview -Feasibility -R&D permissions Dr Alison Walker National Coordinator, NRS Permissions CC Commercial presentation.
NHS Research Scotland - Overview Dr Alison Walker National Coordinator, NRS Permissions CC
1 Contract Closeout Plan. 2 Where we're at GSFC: Backlog of approximately 1,463 expired contracts and Interagency Agreements Undisbursed obligations total.
Office of Grants & Contracts Accounting (OGCA) Financial Status Reporting (FSR) & Final Invoices using the Award Reconciliation & Review Tool (ARRT) 1.
1 NJ Dept. of Health Decision Tree for eIRB Submission Revised: 06/18/2015 Is this research defined as: A systematic investigation which includes research.
Retha Britz Copyright 2013 All rights reserved for this presentation 1 Establishment and functioning of a REC Retha Britz.
1 LSE Certification Process ERCOT August 23, 2006.
Welcome Document Imaging System Training Dial in number: (559) Participant Access Code: #
ACRIS Electronic Submission Overview Topics How to Sign Up How to Submit What Happens after Submission Tips & Suggestions.
Managing Student Documents. What we will cover: Document Basics Document Categories Confidential Documents Document Forwarding Document Approval Document.
NGager Progress/Final Report. MOH: nGager Roadshow Agenda 1.Progress/Final Report Submission on nGager workflow 2.Progress Report on nGager 3.Final Report.
Doctoral Coordinators: Approve for Admission or Waitlist ADMIT.
This is the iInterfolio site: Click on APPLY NOW FOR FREE.
Getting a study done at Jefferson:. Startup Activities: Image courtesy of CITI Program Clinical Research Coordinator course.
UNFCCC secretariat, Sustainable Development Mechanisms programme Nashib Kafle, Associate Programme Officer Session 3: The Concept of Programme of Activities.
1 NJ Dept. of Health Decision Tree for eIRB Submission Revised: 01/25/2016 Is this research defined as: A systematic investigation which includes research.
NEW BUSINESS APPLICATION PROCESS FOR ON-LINE APPLICATION FORMS FPA Loads application form on Discovery Health on-line system Loads application form on.
DUE PROCESS, MEDIATION & AGENCY COMPLAINTS Elvin W. Houston December 7, 2011.
Reciprocity Agreement Programs at WVU For residents of Garrett County, Maryland, and the State of Ohio Academic Common Market (ACM) at WVU.
EDE Welcome Page 1. Request Documents page 2 Select Documents to Request page 3.
© 2016 University at Buffalo Click Training Agreements Module University at Buffalo Office of the Vice President for Research and Economic Development.
Site Set-up and Conduct Caroline O’Leary and Carrie Bayliss.
Submitting to a Commercial IRB Kyle Conner, MA, CIP Associate Director Office of Human Research.
“Are We Ready? ” Research Administration Day 2016 Research Services Office Together we make it happen Research Administration Day June 1, 2016 “Are we.
District Validation Review (DVR) Nonpublic School Preparation Information Division of Special Education.
Eligibility Process for Cohort 4 & 5 HRA Approval Studies (post CSP) RM&G Lead’s 09 March 2015 Louise Lambert: Non-commercial Research Initiatives.
Decision Tree for eIRB Submission Revised: 01/25/2016
PERMISSIONS COORDINATING CENTRE
E2 Revisions How to revise an eDMR that has been rejected by a signatory or a member of DEQ.
Decision Tree for eIRB Submission Revised: 01/12/2016
Doctoral Coordinators: Approve for Admission or Waitlist
Decision Tree for eIRB Submission Revised: 01/25/2016
Commissioning Manager Commissioning Support Assistant
Process Describing the Pathway from Initial IRB Submission of a Protocol to Approval of a Study Site Agreement (SSA) and Distribution of Site Agreement.
Grant Solicitation System (GSS) Tutorial for Applicants
Bringing Home the Bacon: Grant Writing Basics Unit 7 Grant Submission
PERMISSIONS COORDINATING CENTRE
Click Training Agreements Module
Commissioning Manager Commissioning Support Assistant
External moderation and certification
AURA IBC Fundamentals.
Post-Award Grant Administration
Interview •The Zone Clinical Director interviews the NR
Facility Asset Data Exchange (FADE) Design Phase
Award Management A Compliance Hold is system generated by eRPM if required system check approvals are missing. Once the compliance approvals are completed,
UK-wide study: (lead R&D office in other UK nation) (Non-commercial)
ACCORD UPDATE EVENTS 2019 Sponsorship and R&D
UK-wide study (lead R&D office in Scotland)
Introducing eCentral Seminar
Process flow Kindly note: This presentation is automated – please do not click any of your mouse buttons or keyboard keys.
Process: Scotland only study (multicentre)
Informal document GRE-76-02
Knowledge Hub: Connections.
USF Research Integrity & Compliance
Using the AIM Alternative Testing Module (for Instructors)
NRS R&D permissions process Scottish sites only, multicentre
Using the AIM Alternative Testing Module (for Students)
Compliance Manual Update Staff Requirements Check
Grant Agreement Preparation
UK-wide study (lead R&D office in other UK nation)
NRS R&D permissions process Scottish sites only, multicentre
Presentation transcript:

R&D Permissions Process (multicentre) Notification Application Check Review R&D Permission Full document set Applicant notifies NRS Permissions CC NRS Permissions CC sends Document Submission Checklist Certificate of Compliance (CofC) Applicant sends IRAS R&D application to NRS Permissions CC And IRAS SSI Forms to PIs NRS Permissions CC checks / uploads document set onto SReDA; notifies participating R&D offices; requests outstanding documents Generic Review Local Management permission letter Local Review(s) SSI Forms Confidentiality Agreements as required NRS Permissions CC will confirm when we have a full document set