Scope
This paper applies to biopharmaceutical, bulk pharmaceutical and finished dosage form operations;
liquid, dry, solid and semi-solid dosage forms are covered in both sterile and non-sterile presentations.
Both clinical and marketed product cleaning validation programs are identified
This paper applies to biopharmaceutical, bulk pharmaceutical and finished dosage form operations;
liquid, dry, solid and semi-solid dosage forms are covered in both sterile and non-sterile presentations.
Both clinical and marketed product cleaning validation programs are identified
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