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All essential documentation will be stored as specified under the guidance from the clinical trials unit.
All relevant documentation will be stored along with the patient notes as stipulated within the NHS framework.
Data and all appropriate documentation will be stored for a minimum of 5 years after the completion of the study, including the follow-up period.
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Written informed consent will be obtained from each patient in order to allow data and sample collection for storage in a central databank and biobank; additionally photo documentation as well as skin and other specimen will be stored when available.
Paper-based documentation, such as consent forms collected during recruitment and questionnaires, will be stored until 31 March 2017 (the end of the study period), after which they will be shredded and disposed of.
The data set will be stored in a computerised database and study documentation and materials (including informed consent forms) will be stored in locked file cabinets when not in use at APHRC.
The Principal Investigator or delegate will maintain source documentation for every participant enrolled in the study and all study forms for each enrolled participant will be stored securely in locked cabinets and will only be accessed by appropriately trained research staff.
will be stored in the GP-practice and will be made available for the practice documentation.
Additionally, plasma will be stored for biobanking.
The urine will be stored frozen.
Data will be stored for 15 years.
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