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    FDA COMPLIANCE 2012 - Understanding Disinfection and Cleanroom Cleaning in a FDA Regulated Environment

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    Website http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701767?channel=ourglocal | Want to Edit it Edit Freely

    Category Disinfectant Validation Training; Cleanroom Cleaning Training; FDA Disinfectant Regulations; EMEA Disinfectant Regulations; FDA Cleanroom Cleaning; EMEA Cleanroom Rules

    Deadline: March 16, 2012 | Date: March 16, 2012

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

    Updated: 2012-01-23 14:56:05 (GMT+9)

    Call For Papers - CFP

    This 90-minute webinar on Disinfection and Cleanroom Cleaning will cover effective ways to rotate disinfectants, most current industry methods for applying disinfectants and effective methods for controlling residues

    Why Should You Attend:

    Designing an effective cleaning and disinfection program is a critical part of your facility operations and contamination control program to meet FDA, EMA, and MHRA regulations. This process involves selecting the most effective products against your isolates, rotating these products, and having a safe and effective method to apply these products. oday end users typically struggle with how often to rotate products and determining exactly which products to rotate.


    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.