This section contain materials useful to learn how to manage an Innovation Project
Published by ECRINTranspariMED
ToolboxClinical Trials ToolkitCollection of hands-on tools and case studies that universities and other institution can use to improve their registration and reporting of clinical trials.
View this resource Bookmark this resourcePublished by National Institute for Health and Care Research (NIHR)ECRIN
Clinical Trials ToolkitThis guidance summarises what an under-served group is, a roadmap suggesting intervention points to improve inclusion, examples of under-served groups and barriers to inclusion
View this resource Bookmark this resourcePANDA is aimed at trialists and researchers in clinical trials who are keen to learn about adaptive designs, their practical application, potential benefits and limitations. The target audience includes, but is not limited to, trial statisticians, clinicians, health economists, grant proposal developers, trial managers, data managers, and reviewers of grant applications
View this resource Bookmark this resourcePublished by ECRINPediatric musculOskeletal & RheumaTology Innovation COre center
ToolboxClinical Trials ToolkitThe toolkit is a curated series of publicly accessible videos and links covering essential operational details that early investigators need to know before embarking on a clinical trial with a special focus on pediatric trials. Topics address study startup, study documents, consent, oversight, management, and safety.
View this resource Bookmark this resourcePublished by The Global Health NetworkECRIN
TemplatesClinical Trials ToolkitDeveloped by the Global Health Trials Knowledge Hub , this library of templates includes clinical trials´ general logs and trackers, documents for finances management, patients enrolment and study, site and staff management
View this resource Bookmark this resourcePublished by GoodtrialsECRIN
Clinical Trials ToolkitGuidelineThe guidance is intended to support all individuals and organizations involved in the planning, conduct, analysis, oversight, interpretation, funding, and regulation of RCTs of any health intervention for any purpose in any setting.
View this resource Bookmark this resourceWhen you plan in reverse, you start with your end goal and then work your way backwards from there to develop a plan of action. Working backwards in this way can give you a much clearer picture of what and how much must be accomplished during each phase of a project. It can also help you identify and avoid unnecessary activities
View this resource Bookmark this resourceA target product profile (TPP) outlines the desired characteristics of a new drug or other medical intervention (e.g diagnostic tool). TPPs describe intended use, target populations and other desired attributes of products, including safety and efficacy-related characteristics. In industry TPPs are used as planning tools that guide development towards desired characteristics. In the regulatory context, TPPs are considered as tools to frame development in relation to submission of product dossiers.
View this resource Bookmark this resourceThis guide helps you understand what technology transfer is in the context of university and research institutions
View this resource Bookmark this resourcePublished by IRDiRC
Advisory Committee for TherapeuticsTREAT-NMDEstablished in 2009, the TREAT-NMD Advisory Committee for Therapeutics (TACT) is a unique multi-disciplinary international group of internationally recognized academic and industry drug development experts as well as representatives of patient foundations and regulatory experts
View this resource Bookmark this resource
