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    Live event FDA Auditing Practices and the Top 10 Most Common Cited GMP Deficiencies

    View: 225

    Website https://compliance2go.com/product/?pid=CP2014-415 | Want to Edit it Edit Freely

    Category Biotechnology ;Medical Device ;Pharmaceutical

    Deadline: February 17, 2015 | Date: February 18, 2015

    Venue/Country: Online, U.S.A

    Updated: 2015-01-23 17:45:40 (GMT+9)

    Call For Papers - CFP

    DESCRIPTION

    The success of getting through any audit by federal regulators is not only dependent on a well prepared training of all staff and department employees, but also in knowing what the focus has been of recent inspections within the industry. Such information provides a template for companies to look closely at their own practices in helping to assure similar findings are adequately addressed. In addition, as the audit techniques of the FDA have changed over the years, knowing what to expect can help establish a focused training program as part of the preparation.

    This webinar will look as changes in the FDA’a approach to audits and the current method used by the agency to determine audit frequencies by using a system of “risk assessments”. The top 10 most cited GMP deficiencies over the last year will be reviewed along with the significant increase in the number of warning letters issued over the last 4 years. Actual case examples will be used to highlight various points discussed and attendees will get a chance to ask questions throughout the presentation

    Why you should attend:

    This webinar will provide the attendees with a better understanding of the current audit techniques used by the FDA and how they have changed over the years. Additionally, the webinar will provide a template that companies can use to evaluate their own state of compliance by knowing what have been the most common cited GMP deficiencies over the last year.

    Areas Covered In the Seminar:

    Changes in FDA audit approaches

    Most common cited GMP deficiencies for 2011-2012

    Increase in FDA enforcement actions

    Who will benefit:

    Quality Assurance

    Quality Control

    Manufacturing

    Production

    Regulatory

    Laboratory Personnel

    Management

    Webinar Includes:

    Q/A Session with the Expert to ask your question

    Copy of PowerPoint slides (PDF print only)

    90 Minutes Live Presentation

    Certificate of Attendance


    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.