Indicates successful development of key trial documents. Submission to EC in accordance with EC H2020 clinical trial requirements.
Project Data Management Plan
To document clearly how information about CHILTERN will be disseminated to all partners and participants during the project. This will also involve WP leads who will be responsible for providing information about their WP.
Protocols for standardised collection of clinical samples and sample analysis
To document clearly how the results from all the work packages will made available to the appropriate audiences; including clinicians, researchers, patients and the public
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