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In a 2018 guidance, FDA explained that it would consider a compounded drug to be essentially a copy of a commercially available drug if it has (i) the same API, (ii) the same or similar dosage, and (iii) the same route of administration, unless a prescriber determines that there is a change, made for an identified individual patient, which produces, for that patient, a significant difference from the commercially available drug product. The guidance also explains that, if a change is made for an identified patient, the prescriber should document the determination on the prescription, and the notations should be specific

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Survodutide : Phase 2 completed for obesity (Lancet 2024) and MASH (NEJM 2024)

The only authoritative source is your clinical trial protocol, study sponsor, or dispensing pharmacy there is no NHS or NICE guidance available for this compound

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First, immunoassays provide a qualitative yes or no answer to whether the drugs being tested for are present in the biological sample