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- Posts: 29
- Joined: Wed Dec 22, 2004 4:38 pm
We've recently begun using a new excipient (flavoring) in a pharmaceutical oral dosage form. The CofA from the manufacturer lists "Total Sugars" with "Trace" as the specification limit. Their analytical method is via colorimetric titration.
My question: How does one objectively quantitate "Trace?" Is th a compendial (USP, EP...) definition out there somewhere? I've spoken to the vendor and they indicate that their actual result is usually "not detected" and since they haven't used this particular material in pharma products this issue has never come up for them.
Any thoughts?
Thanks,
Jeff
