This is TREAT-NMD webpage, where it can be found relevant information how to find biomaterials for The basic scientific research being carried out on Neuromuscular Diseases. It can work also as inspiration for investigators conduting reasech in others rare diseases
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Advisory Committee for Therapeutics (ACT) toolkit – Full application form
Published by TREAT-NMD
TemplatesTranslational ResearchResearch and Drug DevelopmentTREAT-NMDClinical DevelopmentClinical Trial DesignPreclinical ResearchAdviceOnce the pre-application form has been accepted, the applicant will be asked to submit a more detailed application form. This will ensure that the review panel will have sufficient information to be able to comprehensively review the application for advice. Depending on the disease area, the core committee should agree consensus on the questions to be included as part of an ACT application form.
This report to the applicant template can be used in conjunction with the ACT toolkit. For further information, please see the ACT toolkit.
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SPIRIT PRO Extension for inclusion of patient-reported outcomes in clinical trials protocols
Published by ECRIN
Clinical Trials ToolkitPCOMExtension of the SPIRIT (Standard protocol items: recommendations for interventional trials) guideline, SPIRIT PRO provides guidelines for inclusion of patient-reported outcomes in clinical trial protocols.
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TranspariMED: Clinical trial transparency tools
Published by TranspariMEDECRIN
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.
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Improving inclusion of under-served groups in clinical research: Guidance from INCLUDE project
Published 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
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PORTICO Clinical Trials Toolkit
Published by ECRINPediatric musculOskeletal & RheumaTology Innovation COre center
Clinical Trials ToolkitToolboxThe 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.
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Global Health Trials Tools and Templates library
Published by ECRINThe Global Health Network
Clinical Trials ToolkitTemplatesDeveloped 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
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Guidance for good randomized trials (The Good Clinical Trials Collaborative)
Published by ECRINGoodtrials
GuidelineClinical Trials ToolkitThe 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
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