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HiI am trying to find out about the Regulations for the use and management of Controlled Drugs within the pharmaceutical manufacturing process. I was an experienced Controlled Drug Accountable Officer (in a PCT) and I am fully aware of the Controlled Drugs (Supervision of Management and Use) Regulations 2013 and how they relate to management roles and systems and processes within healthcare provider organisations.What I am trying to find out is if there is an equivalent “CDAO” role, with associated Regulations when Controlled Drugs are used throughout the manufacturing process. Any help or relevant resources gratefully received
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