Disinfectant Qualification l Disinfectant validation in pharmaceutical industry l Efficacy testing.

Disinfectant Qualification l Disinfectant validation in pharmaceutical industry l Disinfectant Efficacy
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Disinfectant Qualification l Disinfectant validation in pharmaceutical industry l Disinfectant in pharma company
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Questions covered :
Q. In simple words what is disinfectant qualification / disinfectant validation?
Q. What are the key steps of disinfectant qualification?
Q. What are the key components of disinfectant validation protocol ?
Q. What are the typical challenge organisms during disinfectant validation ?
Q. What is disinfectant contact time?
Q. What is term “Residual effect”, “Zone of Inhibition” and “Minimum Inhibitory Concentration (MIC)”?
Q. What is the disinfectant manufacturer role and end use role in the disinfectant qualification ?
Q. What are the key tests that performed during disinfectant validation study ?
Q. On which surfaces / materials disinfectants are commonly tested ?
Q. What are the different class of disinfectant used in the pharmaceutical industry ?
Q. When we should perform disinfectant qualification?
Q. What acceptance criteria is generally followed for disinfectants in pharmaceutical industry?
Q. What surface properties impact on disinfectant efficacy?
Q. What spectrum of activity generally expected from disinfectants in pharmaceutical industry ?
Q. What is coupon in the context of disinfectant Qualification ?
Q. How coupons are used during disinfectant qualification / validation ?
Q. What are the important factors that need to be considered during disinfectant validation ?
Q. What are key micro-organism we should challenge during disinfectant qualification?
Q. Which external labs perform disinfectant qualification for pharmaceutical industries?
Q. What are the guideline referred for disinfectant qualification in pharmaceutical industry?

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Keywords to find this video:
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