Regulatory Reference for Controlled Drug Manufacturer

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biggwaltz1

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Hi all. I just started a new role auditing third party suppliers for my current company. One of the suppliers is a manufacturer of an opioid. Are there are any specific regulatory references besides the general 21 CFR Parts 210/211 that are usual used as part of the inspection? I want to evaluate the controlled drug processes (including procedures and security measures), but am not sure if there is a specific guidance I should reference. I welcome any feedback.
 
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