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    FDA COMPLIANCE 2012 - Understanding Disinfectant Qualification Studies ? How to Avoid Errors

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    Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702210?channel=ourglocal | Want to Edit it Edit Freely

    Category Disinfectant Qualification Studies; Disinfectant Validation; Regulatory requirements for disinfectants; disinfectant testing methodologies

    Deadline: March 01, 2012 | Date: March 01, 2012

    Venue/Country: Palo Alto, U.S.A

    Updated: 2011-12-26 17:52:26 (GMT+9)

    Call For Papers - CFP

    This 90-minute webinar on Disinfectant Qualification Studies will teach you disinfectant testing methodologies, provide examples of disinfectant efficacy tests and show how to troubleshoot problems related to disinfectant efficacy testing.

    Why Should You Attend:

    How do you design an effective disinfectant validation program that meets FDA , MHRA, EMA scrutiny?

    This webinar provides guidance on industry trends, regulatory feedback, and designs for an effective validation program. Current 483's, Warning Letters, and Field Experiences will be conveyed that allow end users to determine the best methods to validate their products against their isolates.


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.