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    GMP Compliance Audit: How Best to Prepare for it

    View: 331

    Website https://compliance2go.com/product/?pid=CP2014-416 | Want to Edit it Edit Freely

    Category Biotechnology , Medical Device , Pharmaceutical

    Deadline: March 12, 2015 | Date: March 12, 2015

    Venue/Country: Online, U.S.A

    Updated: 2015-02-27 17:34:05 (GMT+9)

    Call For Papers - CFP

    DESCRIPTION

    Companies today regulated by the FDA are increasingly aware of the enforcement actions by the agency with respect to regulatory compliance. This webinar will highlight the 10 most common GMP deficiencies cited by auditors in 2011, along with the significant increase in warning letters issued over the last 3 years. The review of such information lays the groundwork for which companies can use to evaluate their own state of compliance and how best to prepare for such an audit. The webinar will briefly examine each of the deficiencies and where companies fall short in meeting the regulatory requirements.

    In addition to the most common GMP deficiencies given to industry in 2011, the webinar will also help attendees in preparing an audit checklist that can be used to evaluate their own state of compliance. Attendees will be given several steps that can be used to help avoid regulatory trouble in this time of enforcement activities. Attendees will also be given the opportunity to ask questions and actual case examples will be discussed to highlight some of the topics covered. This webinar is a wealth of information for those involved with supply chain activities, manufacturing, validation and quality assurance to name a few.

    Why you should attend:

    This webinar will provide the attendees with a checklist of the most common areas of focus by regulatory auditors during GMP Compliance Audits. With an ever increasing number of recent warning letters and Consent Decrees issued in the last several years, companies must know what inspectors are focusing on and how best to evaluate their own state of compliance. Preparation is a key factor to successfully get through an audit and this webinar will give attendees some valuable tips to achieve this.

    Areas Covered In the Seminar:

    Review common and recent industry cited GMP deficiencies.

    Discuss common mistakes made by industry relative to deficiencies noted.

    Review topics to include for an audit checklist to evaluate your company’s state of compliance.

    Discuss how to help avoid regulatory trouble.

    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.