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    Expectations of Regulatory & Validation Master Planning - 2017

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    Website http://www.compliance4all.com/control/w_product/~product_id=501357LIVE?channel=ourglocal_Jul_2017_SE | Want to Edit it Edit Freely

    Category Validation Master Planning, Quality System Documentation, Pharmaceutical Industries, Quality Assurance, Quality Control, Validation, validation master plan software, Regulatory expectations

    Deadline: July 19, 2017 | Date: July 20, 2017

    Venue/Country: Online, U.S.A

    Updated: 2017-05-16 20:29:45 (GMT+9)

    Call For Papers - CFP

    Overview:

    This presentation will cover the importance of master planning. The FDA and other regulatory bodies expect these to be among the Quality System documentation.

    Areas Covered in the Session:

    History and background

    Types

    Organization

    Requirements

    Regulatory expectations

    Maintenance

    Who Will Benefit:

    Compliance Personnel

    QA Personnel

    validation Personnel

    Speaker Profile:

    Louis Angelucci is a pharmaceutical professional and Certified Quality Engineer with over 20 years of experience in Quality Assurance, Quality Control, Validation, consent decree remediation as well as cGMP Compliance in the Medical Device and Pharmaceutical industries.

    Contact Detail:

    Compliance4All DBA NetZealous,

    Phone: +1-800-447-9407

    Email: supportatcompliance4All.com


    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.