Dear All,
I have been asked by the Adult Social Care Department regarding the DPA
implication of external researchers using Client data held by the
authority for research under the Department of Health "Research Governance
Framework" policy.
To protect ourselves I feel we need to create a ISA with the researcher to
outline the provisons for which the data may be used, stored, published
and destroyed? Does anyone have such a DP Research Agreement they would
like to share?
Any advice would be welcomed.
Many Thanks,
Tom
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