UK-wide study (lead R&D office in Scotland)

Slides:



Advertisements
Similar presentations
OJT – On the Job Training Time Cards - State Board of Education Rules Chapter 6A-1.044(6)(c) The attendance of a pupil who is assigned to an on-the-job.
Advertisements

Research Policy & Management RACD INTRODUCTION TO RESEARCH GOVERNANCE.
Quality Education for a Healthier Scotland How to assign Appraisers to Appraisees For Local Administration Teams (Secondary Care)
Health Care Information Consultants, LLC Meaningful Use Pre-Payment Audit Jennifer Moore, MHA Principal May 16, 2014.
Quality Education for a Healthier Scotland How to assign Appraisers to Appraisees For Local Administration Teams (Primary Care)
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.
Multi-Institutional Facilitated IRB Review Philip A. Cola, MA Vice President, Research and Technology University Hospitals Case Medical Center Third Annual.
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.
Uploading a Turnitin Assignment Faculty of Humanities and Social Sciences.
National Institute for Health Research Coordinated System for gaining NHS Permission (NIHR CSP) A single system for processing and reviewing applications.
SP Attach for Outlook and SharePoint A better way to send files SP Attach works with Outlook 2007 and above and SharePoint 2010, 2013.
Research and Development 07/05/2015 Bala Thirugnanabalan & Dale Batham.
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.
1 LSE Certification Process ERCOT August 23, 2006.
 Understanding the IRB Process University of Tennessee Health Science Center Institutional Review Board.
1 Defense Health Agency Privacy and Civil Liberties Office HIPAA Privacy Board Overview August 6, 2015.
TETF Workshop. Agenda Eligibility Applying for the Award Application process and submission guidelines.
Cardiff and Vale UHB Bwrdd lechyd Prifysgol Caerdydd a’r Fro NHS R&D Overview How to avoid the common pitfalls? Thomas Fairman Research Liaison Manager.
Human Subjects Research Cynthia Edmonds Director, Office of Research Support Committees.
Where does R&D fit? Dr Clara Kalu Senior Portfolio Co-ordinator UCL Students’ Research.
Innovation 2007, Prague, 4 December 2007 Procedure to submit an application Svatopluk Halada.
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.
How to submit an assignment to Turn It In Log in to Turn It In and select the class Find the assignment to be submitted Click “Submit”
Accessing the NHS for Research – NHS R&D Permissions Jemma Hughes R&D Manager ABMU Health Board.
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.
Letter of Authorization and Line of Credit Date: To:Debbie Lemmon Information Technology Management Office Division of the State CIO From:Company Contact.
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.
District Validation Review (DVR) Nonpublic School Preparation Information Division of Special Education.
HRA Approval: training for non-commercial studies
London (South) Comprehensive Local Research Network
Applying for ethical approval
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
INDUSTRY ALIGNMENT FUND – PRE-POSITIONING PROGRAMME LETTER OF INTENT
PERMISSIONS COORDINATING CENTRE
Decision Tree for eIRB Submission Revised: 01/12/2016
INDUSTRY ALIGNMENT FUND – PRE-POSITIONING PROGRAMME LETTER OF INTENT
Decision Tree for eIRB Submission Revised: 01/25/2016
Process Describing the Pathway from Initial IRB Submission of a Protocol to Approval of a Study Site Agreement (SSA) and Distribution of Site Agreement.
USOAP Continuous Monitoring Approach (CMA) Workshop
eMedical User Roles Guide
INDUSTRY ALIGNMENT FUND – PRE-POSITIONING PROGRAMME LETTER OF INTENT
Getting a Study Done at Jefferson:
PERMISSIONS COORDINATING CENTRE
DRS Replacement IT System
Click Training Agreements Module
R&D Permissions Process (multicentre)
ACCORD Update/Training Event The Changing Research Landscape 26th February 2019 Heather Charles Head of Research Governance.
UK-wide study: (lead R&D office in other UK nation) (Non-commercial)
ACCORD UPDATE EVENTS 2019 Sponsorship and R&D
Process flow Kindly note: This presentation is automated – please do not click any of your mouse buttons or keyboard keys.
ADDITION OF DEPENDANT APPLICATION PROCESS
Process: Scotland only study (multicentre)
USF Research Integrity & Compliance
INDUSTRY ALIGNMENT FUND – PRE-POSITIONING PROGRAMME LETTER OF INTENT
NRS R&D permissions process Scottish sites only, multicentre
Sleep SMART Clinical Trial Agreements / Regulatory Webinar
IRB submissions for researchers
UK Wide Working Mary Cubitt Programme Implementation Manager
UK-wide study (lead R&D office in other UK nation)
NRS R&D permissions process Scottish sites only, multicentre
Presentation transcript:

UK-wide study (lead R&D office in Scotland) Applicant notifies Permissions CC of UK-wide multicentre project Permissions CC sends applicant ‘Document Submission Checklist’ Confidentiality Agreements as required Applicant sends IRAS R&D application to Permissions CC; and IRAS SSI Forms to PIs (UK-wide) Permissions CC uploads documents to SReDA; notifies participating Scottish R&D office(s); requests outstanding documents; assigns lead reviewer Permissions CC emails IRAS R&D Form to other UK nation(s) Generic Review Local Review(s) Scottish sites SSI Form Permissions CC emails global documents to other UK nation(s) Certificate of Compliance (CofC) Permissions CC emails CofC to other UK nation(s) For each Scottish Health Board: Local management permission letter Permissions CC will confirm when we have a full document set

Feedback: Privacy Policy Feedback
Do Not Sell My Personal Information
About project: SlidePlayer Terms of Service

© 2025 SlidePlayer.com. Inc. All rights reserved.