DATA PRESERVATION AND SHARING INITIATIVE. 1. Aims of the EORTC QLG Data Repository project

Similar documents
Ethical Review Manager. Applicant User Guide

PANORAMA Data Security & Access Protocol

LOUGHBOROUGH UNIVERSITY RESEARCH OFFICE STANDARD OPERATING PROCEDURE. Loughborough University (LU) Research Office SOP 1027 LU

Scientific Research Data Management Policy

eirb Electronic Institutional Review Board User Guide For more information contact: Research Administration (803)

Developing a Research Data Policy

Checklist and guidance for a Data Management Plan, v1.0

University of California, San Francisco Helen Diller Family Comprehensive Cancer Center Policy and Procedure. PRMS Amendment Submission Policy

EBMT. European Society for Blood and Marrow Transplantation. Version 5.2. Last review 02/02/2018

Velos ecompliance. Researcher User Manual

Student Guide. Click here to log in. A: Log in

SUBMITTING AN ANNUAL PROGRESS REPORT FOR PRINCIPAL INVESTIGATORS

!"# $ # # $ $ % $ &% $ '"# $ ()&*&)+(( )+(( )

OnCore Enterprise Research. Subject Administration Full Study

ENCePP Code of Conduct Implementation Guidance for Sharing of ENCePP Study Data

NEWCASTLE CLINICAL TRIALS UNIT STANDARD OPERATING PROCEDURES

Researchfish outcome reporting system. User Guide for Researchers

Nova Scotia Health Authority Research Ethics Board. Researcher s (PI) User Manual

Researcher User Manual

GIF Submission Website - Instructions How to Fill In your Online Application in the GIF Regular Program

Office of Human Research

The Lilly Safety Mailing Process

Cancer Clinical Trials Centre Standard Operating Procedure

SOP Owner: Finance Last Reviewed/Update Date: 10/05/2015. Petty Cash Reimbursement on Grants Standard Operating Procedure

Logging in, Navigating, & Finding your study

Research Data Management Procedures and Guidance

Basic Requirements for Research Infrastructures in Europe

Investigator Activities Quick Reference Guide. Sanofi/Genzyme October 2013

ERM User guide. The Royal Children s Hospital, Melbourne

Data Management Checklist

ACCREDITATION COMMISSION FOR CONFORMITY ASSESSMENT BODIES

ROCHE/GENENTECH PRACTICAL WORKING GUIDE FOR REQUESTORS

Document valide au 21/08/2015. Welcome Booklet

eirb User Manual for Research Staff

TIES Usage Policies. for University of Pittsburgh. Authors. University of Pittsburgh

Patient Evaluation and Management System (PEMS) User s Guide

Data Management Plan Generic Template Zach S. Henderson Library

Application form guidance

ACCAB. Accreditation Commission For Conformity Assessment Bodies

Activity Director Portal Online Application 2017 Reference Guide

APPENDIX TWO RETENTION AND DISPOSAL SCHEDULE IMPLEMENTATION GUIDELINES

APPENDIX THREE RETENTION AND DISPOSAL SCHEDULE IMPLEMENTATION GUIDELINES FOR NSU PROVIDERS

Chapter 10: Regulatory Documentation

University of Pennsylvania Institutional Review Board

Idealist2018 Project. Ideal-ist Partner Search System - Manual for Proposers

Workshop MedSciNet - Building an Electronic Data Capture System for a Clinical Trial

CTP SUBMISSION PLATFORM

Vaccine data collection tool Oct Functions, Indicators & Sub-Indicators

STANDARD OPERATING PROCEDURE SOP 815. Clinical Data Management System LOCKING AND UNLOCKING THE DATABASE. Joint Research Office

RPg procedures for Research Data Management (RDM)

ELECTRONIC SITE DELEGATION LOG (esdl) USER MANUAL

Focus: Themes within Introduction and Context

User Guide for DCP Consortia 2012

Submitting an Protocol for De Novo Review

Reviewers Guide on Clinical Trials

Romeo. How to Apply for a Faculty Conference Travel Grant

Standard Operating Procedure. SOP full title: Sponsor processes for reporting Suspected Unexpected Serious Adverse Reactions

Research Data Use Agreement (RDUA)

WesternREM (WREM) Applicant

This instruction will guide you through all the procedures and activities, necessary for your participation in the trading.

NHS Education for Scotland Portal Dental Audit: A user guide from application to completion

Preparing the Office of Scientific Investigations (OSI) Requests for Submissions to FDA

irb.unm.edu

Completing & Submitted the IRB Approval of Human Subjects Form

Standard Operating Procedure. Data Management. Adapted with the kind permission of University Hospitals Bristol NHS Foundation Trust

INVESTIGATION REPORT , , ,

ACCREDITATION COMMISSION FOR CONFORMITY ASSESSMENT BODIES

AQuIP On-line Accrual Reporting System (OARS) User Guide for DCP Consortia 2012

NSTIP Portal Registration Manual NSTIP Portal Registration Manual

Ethical Review Online Application System: User Guide

User manual for applying online for certification under the Health and Disability Services (Safety) Act 2001

Memorandum of Understanding between the Central LHIN and the Toronto Central LHIN to establish a Joint ehealth Program

January 16, Re: Request for Comment: Data Access and Data Sharing Policy. Dear Dr. Selby:

Online Forms User Manual

Science Europe Consultation on Research Data Management

HRA Open User Guide for Awardees

ipcr Web Training Manual

Using DCC DMPonline to write a Data Management Plan

ORA HIPAA Security. All Affiliate Research Policy Subject: HIPAA Security File Under: For Researchers

CCGT Grant Application System User Guide for Applicants, Reviewers and Co-Signatories

STREAMLYNE GUIDE FOR STUDENTS/PRINCIPAL INVESTIGATORS

Principal Investigator - Setting up a Project Application. Step 1: Click on Add new. Step 2: Select Project Application. Click on Project Application

DataFlow and VIDaaS Workshop

Suspected Cancer Two Week Referral Forms for GPs A step-by-step guide to installing and using the SystmOne Integrated Word forms.

NSF Data Management Plan Template Duke University Libraries Data and GIS Services

Site User Guide. Oracle Health Sciences InForm CRF Submit Release Part Number:E

Maine ASO Provider Portal Atrezzo End User Guide

Video Services Forum Rules of Procedure

REDCap Longitudinal Studies Class (201) September 20, 2017

Bring Your Own Device Policy

A GUIDE TO USING TASKS

Work Instruction Study Startup

EPA Research Programme EPA s Online Grant Application & Project Management Portal

Researcher User Manual

The MovingLife Project

Security Overview of the BGI Online Platform

Institutional Animal Care & Use Committee Protocol Review

Researchfish Administrator Dashboard Quick Start Guide

Data Management Dr Evelyn Flanagan

SETUP GUIDE PPP FOR PPP USERS PLANT PROTECTION PRODUCTS VERSION 0.4

Transcription:

DATA PRESERVATION AND SHARING INITIATIVE 1. Aims of the EORTC QLG Data Repository project The European Organisation for Research and Treatment of Cancer (EORTC) Quality of Life Group Data Repository project aims to 1) create a central dataset for storage of all field studies data, and 2) establish guidelines to be used to harmonize the way field studies are conducted and the way data for field studies are collected. 2. Definitions Data Repository: a place where data from field studies are stored and maintained over time. In order to create such a repository it is necessary to collect all the available information that concerns the different steps of a field study and to create a central dataset where all the data used for field testing will be stored. EORTC Quality of Life Department (QLD): a department within the EORTC, whose objectives are to evaluate the importance of various factors that improve the Quality of Life (QoL) of cancer patients, to supervise the evaluation of QoL in selected cancer clinical trials and to encourage physicians to pay greater attention to QoL factors in the treatment of cancer. EORTC Quality of Life Group (QLG): a group within the EORTC, whose mission is to develop measures of patient-reported outcomes in cancer, including health-related QoL, and to promote and coordinate studies concerning the QoL of cancer patients. Principal Investigator (PI) or data sharer: the scientific leader of the original research project (field study) that was funded by an EORTC QLG grant and that yielded data that should be stored and preserved in the Data Repository. New Investigator: the scientific leader of a new research project to be carried out on data already in the Data Repository.

3. Aims of the EORTC QLG data preservation and sharing initiative for field studies EORTC QLG funded research produces different datasets, usually stored and kept by the PIs in different institutions. Making this information available centrally to the EORTC QLG will allow safe and efficient data preservation and possible data use for future cancer research. The aims of our data preservation and data sharing initiative are - to identify and develop generic standards for data collection in order to keep the field study process harmonized - to promote good data preservation strategies - to promote the sharing of data for collaborative, high-quality and ethical new research. 4. EORTC QLG policy on data preservation and sharing for field studies Our data preservation and sharing policy applies to all EORTC QLG funded field studies. 4.1. Funding request When applying for funding for a new study, the PI should include in his proposal a section concerning the data preservation and sharing strategy. The contract with the host institution will include a clause for data sharing. When applying to the Research Ethics Committee for the study, the data sharing information should be included and approval sought. The QLG Executive Committee (EC) should be informed about the submission process. 4.2. Data storage Data will be stored on the EORTC server, in a folder with restricted access. Only the person in charge of the Data Repository project and the head of the EORTC QLD will have access to this folder. 4.3. Data sharing

The EORTC QLG expects data to be available in a reasonable time and manner after completion of data collection. PIs are asked to provide a copy of the final locked dataset. Data sharers should ensure data quality. Shared data should be anonymized, where anonymized data are defined as data from which the participant cannot be identified by the recipient of the information. 4.4. Data transfer Two options are available for data transfer. The anonymized data could be sent by e-mail in a password protected compressed folder or, as an alternative, an existing secured EORTC website could be used. Phase IV grantees who wish to use this second option will be provided with further details by the person in charge of the Data Repository project. Two options are also available for sending the password. The password could be sent in a separate e-mail or it could be provided by telephone. 4.5. Future use of the Data Repository A defined period of exclusive use of the data by the PI for primary research will be established: data should become available as from the moment the phase IV paper has been published, unless the PI of the original research makes a specific request for a longer period and the QLG EC agrees. Sharing should enhance the long-term value of the data, and ongoing research should not be compromised by premature data sharing. After this period the Data Repository will be available to EORTC QLG active members for use in future new studies. PIs who are not currently EORTC QLG active members but who have contributed to the Data Repository with data from their field studies will also have the opportunity to request data from the Data Repository. 4.6. Possible new studies derived from shared data Possible new studies derived from shared data should be subject to approval and provide added value to existing research and meet quality standards and ethical requirements. Applicants should write an application in the form of a short study protocol. The new study will need to be approved by the QLG EC. If the new study is approved, the QLG EC will inform the PI of the original research. The PI will have

the opportunity to give comments and ask for amendments, but it will not be possible for him/her to reject the study proposal because, as specified in the contract template, intellectual property is with the QLG. Collaboration between the data sharer (PI of the original research), the funder (EORTC QLG) and the New Investigator is not mandatory. However, in the interests of research, such collaboration is proposed and encouraged. The PIs will be asked whether they would be interested in contributing to the new study (see publication policy). In cases where the applicant and the PI of the original research are the same person no specific approval from the QLG EC is needed. For possible new research the appropriate regulatory permissions should be obtained. 5. Publication policy In the case of new studies based on shared data, the publication policy for new studies should be part of the submitted research proposal. PIs of the original research will be asked whether they would be interested in contributing to the new study. As such, PIs will have the option of being a co-author if their contribution meets the accepted criteria for authorship. A predefined acknowledgement of the PI will appear in the publication otherwise. The publication must acknowledge the source of the data as belonging to the EORTC QLG Data Repository. 6. Confidentiality of data Shared data in the Data Repository are confidential and will not be released by the funders to third parties. 7. References - EORTC data release policy (http://www.eortc.be/services/doc/policies/default.htm) - MRC data access principles (http://www.mrc.ac.uk/ourresearch/ethicsresearchguidance/dataaccess/index.htm)

- MRC data sharing initiative (http://www.mrc.ac.uk/ourresearch/ethicsresearchguidance/datasharinginitiative/i ndex.htm) - MRC personal information in medical research (http://www.mrc.ac.uk/utilities/documentrecord/index.htm?d=mrc002452) - OECD principles and guidelines for access to research data from public funding (http://www.oecd.org/dataoecd/9/61/38500813.pdf)