Any tell which guidelines refer during qualification of vial washing and tunnel
Fir general principles of qualification and validation you can use WHO guidelines (Annex 4, Supplementary guidelines on good manufacturing practices: validation), and for specific purposes, please refer USFDA guidance for industry ( Sterile Drug Products Produced by Aseptic Processing — Current Good Manufacturing Practice) and EUDRALEX Volume- 4, Annexure -1 (Manufacture of Sterile Medicinal Products) requirements.
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