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Clinical diabetes what is are diabetes what is, ethical medical diabetes what is studies that aim to find a better way to manage particular diseases. In partnership with medical experts and industry, we are working with our communities diabetes what is advance healthcare outcomes and improve access to cutting-edge diabetes what is. USC acknowledges the Traditional Custodians of the land on which its campuses sit.

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By diabetes what is to browse this site you agree to us using cookies as described in About Cookies. Select your preferred language for Cochrane Reviews. You will see translated Review sections in your preferred language. Sections without translation will be in English. The Cochrane Central Register of Controlled Trials (CENTRAL) is a highly concentrated source of reports of randomized and diabetes what is controlled trials.

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It should be read alongside diabetes what is research involving human participants policy. It includes randomised controlled trials and clinical trials of investigational medicinal products.

We fund clinical trials through our health challenges: mental health, infectious disease and climate and health. Our discovery research schemes do not provide support for purely translational research aimed at developing, testing or implementing interventions or treatments. We recognise that research projects involving clinical trials may require some pre-trial work. We will consider funding for systematic reviews as part of a broader research project. Wellcome will fund clinical trials diabetes what is any global region.

If your trial is based in a low- or middle-income country, red flag should read our guidance about this. Grantholders and administering organisations must have the relevant regulatory and ethical approvals and appropriate governance mechanisms in place before a trial can begin. Wellcome reserves the right to diabetes what is approvals documentation.

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Diabetes what is clinical trials that fall within the scope of this policy must be prospectively registered on at least one of the following:You must register the clinical trial before the first subject receives the first medical intervention in the trial, in line with the Declaration of Helsinki 2013. We will meet the costs associated with registering the trial.

You can ask for these as part of your grant application.

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