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Dear Clinical Trial Specialist Colleagues
The RPS Support team are currently receiving a number of queries regarding the use of multiple controlled drugs in clinical trials and issues surrounding design of trial prescriptions, requisitioning documentation and record-keeping (ward + pharmacy) in compliance with controlled drug legislation and Department of Health guidance on controlled drugs in secondary care.
The focus has been on double-blind studies involving multiple arms and the practicalities involved in achieving this. Scenarios where the pharmacy may or may not also be blind have been raised.
We are hoping that this network and this discussion can provide insight, guidance, signposting and the sharing of models on this issue.
Thank you in advance
Wing (on behalf of the RPS Support team)
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