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Sterilization - validation, qualification requirements

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1ISPE Boston ChapterFramingham MA 19Sep20131Sterilization - validation, qualification requirementsDawn Tavalsky2Sterilization - OverviewObjectives Discuss definition of Sterile Briefly describe Sterilization methods Describe approaches to be used for the validation of a Sterilization process using Moist Heat as an example Describe requirements for routine monitoring and control of Sterilization Review issues that are specific to other Sterilization processes23Sterile Products - Overview Certain pharmaceutical products must be sterile injections, ophthalmic preparations, irrigations solutions, haemodialysis solutions Two categories of sterile products those that can be sterilised in final container (terminally sterilised) those that cannot be terminally sterilised and must be aseptically prepared 4Sterilization - OverviewWhat is the definition of sterile ?

Sep 19, 2013 · Installation Qualification • Ensuring equipment is installed as per manufacturer’s specification – considerations for new and existing equipment – specifications for the type of autoclave, construction materials, power supplies and support services, alarm and monitoring systems with tolerances and accuracy requirements

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