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This section includes a number of guides, templates and recommendations which will be of use to members.
Patient registries are broadly recognised as a critical underpinning for improving healthcare through research. As an umbrella organisation for many medical research charities intimately involved in this pursuit,registries are a reoccurring theme. Despite their importance however,in too many cases, registries remain a thing of the future.
Practical advice on developing a patient and public involvement (PPI) strategy for research activities.
A core belief of the MRCG is that charity-funded research should be used for public good; for the benefit of patients and to improve the nation’s health. This document provides guidance on the appropriate way to protect, manage and exploit intellectual property and to publicise research findings, generated in the course of a charity-funded research project.
This is a template code which can be used by patient organisations to guide their involvement with industry. We recommend that organisations adapt it, according to their own situation and needs.
Developed by the Medical Research Charities Group (MRCG)