ICF guidelines developed by the H2020 funded i-consent project. It means to provide information for the development of informed consent on research involving humans
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ICF guidelines developed by the H2020 funded i-consent project. Means to provide information for the development of informed consent on research involving humans
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Regulatory and Ethics Toolkit, ICF guidelines
Published by IRDiRCECRINGlobal Alliance for Genomic and Health (GA4GH)
Clinical Trials ToolkitGA4GH and IRDiRC have developed model consent clauses for rare diseases research, in order to improve data interoperability, to meet the informational needs of participants, and to ensure proper ethical and legal use of data sources and participants’ overall protection
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Guidelines for effective Data Management Plan
Published by ECRINInter-university Consortium for Political and Social Research (ICPSR)
Clinical Trials ToolkitGuidance to create Data Management plans developed by the Inter-university Consortium for Political and Social Research (ICPSR), an international consortium of academic institutions and research organizations.
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Data Management Plan Online
Published by ECRINDigital Curation Centre and California Digital Library
Clinical Trials ToolkitTemplates for data management plans based on the specific requirements listed in funder policy documents.
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Cambridge Clinical trials Unit SOPs and Documents
Published by ECRINCambridge Clinical Trials Units (CCTU)
Clinical Trials ToolkitCambridge Clinical Trials Units SOPs and templates on: pre-trial planning, protocol development, set-up; pharmacovigilance; data management and statistics; sample management; trial management; post-study procedures and archiving
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CTTI implementation tools
Published by Clinical Trials Transformation Initiative (CTTI)ECRIN
Clinical Trials ToolkitCTTI-developed tools to improve the quality and efficiency of clinical trials. Tools include resources to optimize recruitment and informed consent process
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UKTMN Guide to Efficient Trial Management
Published by ECRINUK Trials Management Network
Clinical Trials ToolkitThis guideline describes the process of managing clinical trials and gives an overview of the trial management framework, both legal and operational, providing hints, tips and references to external resources
View this resource Bookmark this resourceThis toolbox contains templates, sample forms, and information materials to assist clinical investigators in the development and conduct of high-quality clinical research studies
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How to Plan and Manage a Project
Published by ANU Press
Translational ResearchResearch and Drug DevelopmentProject ManagementThis Research management manual describes the rules and procedures that are required to successfully conduct translational research programmes . Depending on the nature and the complexity of a given project an increasingly complex and thorough project planning is required.
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