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    ASEPTIC PROCESSING, FACILITY DESIGN, ENVIRONMENTAL 2017 - How you can prevent microorganism contamination - By AtoZ Compliance

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    Website http://bit.ly/2nVH0H7 | Want to Edit it Edit Freely

    Category site master file fda, fda environmental monitoring, fda ectd, gmp webinar, cgmp audits, pharmaceutical compressed air-quality gmp requirements, equipment validation plan, fda system validation, computer system validation fda, tmf in clinical research, fda validation training, fda gmp compliance, fda cgmp compliance

    Deadline: April 04, 2017 | Date: April 04, 2017

    Venue/Country: Online, U.S.A

    Updated: 2017-03-27 18:51:23 (GMT+9)

    Call For Papers - CFP

    April 04th, 1:00 PM - 2:00 PM EDT

    If prevention of microorganism contamination applies to your business, then we have the right module for you in this webinar.

    This session will review the corrective and preventive action FDA procedure involving the use of specialized equipment in a clean room. Understand;

    • The definition of Aseptic processing

    • Terminal Sterilization vs. AP

    • Facility design and how it impacts the product

    • Proper environmental monitoring

    Why Should You Attend:

    This environmental control in pharmaceutical industry webinar is a good refresher for those personnel that are familiar with the way to properly work in the clean room and why environmental control rooms are designed for proper contamination control.

    Areas Covered In This Webinar:

    In sterile compounding, aseptic technique is contributing to the prevention of microbiological contamination. It is providing sterility, safety, and efficacy to the sterile product, especially various injections for patients.

    Cleaning, Gowning and proper methods of contamination control will be reviewed keeping in mind FDA audit training, FDA CGMP compliance and FDA environmental monitoring, along with why clean rooms are designed the way they are.

    Instructor Danielle DeLucy, is the owner of ASA Training and Consulting, which provides Pharmaceutical and Biologics companies with assistance to meet regulatory compliance.

    At AtoZ Compliance, we focus on our core values - quality, expertise, and customer experience which are the foundation of our business. We take extreme care in selecting topics which are highly relevant to you.


    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.