someone explain 503A to me like I have not read a paper in years
someone explain 503A to me like I have not read a paper in years. I would rather ask a basic question now than get this wrong quietly for two months. Asked which facility and got a name straight away. Looked it up, found the registration, felt considerably better about the whole thing. The intake asked me three…
potency testing on the finished preparation is the thing to ask for
Removed the staff name. Facilities and clinics can be named here; individuals cannot.
Compounded preparations are not approved products and carry no bioequivalence claim. That is a statement about regulatory category, not about quality.
Correction: patient-specific refers to the prescription, not to a bespoke formulation. Common misreading and it changes the argument.
Same view. If the intake asked you nothing, the intake was a formality and you should factor that in.
Nothing in this thread is medical advice, and the choice between arrangements is one for you and a prescriber who knows your history.