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    How to Meet FDA QSR and ISO 13485 Requirements - 2017

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    Website http://www.compliance4all.com/control/w_product/~product_id=501264LIVE?channel=mailer&camp=Webinar&A | Want to Edit it Edit Freely

    Category Food And Drug Administration, Fda Drugs, FDA 2017, fda regulations, supply chain manager, supply chain logistics management, compliance risk, regulatory risk, FDA, Supplier Evaluation and Assessment, QSR Regulations

    Deadline: April 30, 2017 | Date: May 01, 2017

    Venue/Country: Online, U.S.A

    Updated: 2017-03-21 16:15:31 (GMT+9)

    Call For Papers - CFP

    Overview:

    A lack of adequate control over purchases has resulted in a significant number of recalls due to component failures. Since FDA does not directly regulate component suppliers, it is imperative that your company's purchasing and supplier control requirements provide the assurance that only acceptable components are used to manufacture finished devices.

    Why should you Attend:

    This presentation will review the QSR and ISO requirements for supplier evaluation and assessment. It will also provide cost efficient and equally compliant options for many of the most common practices in supplier management programs.

    Areas Covered in the Session:

    QSR and ISO requirements for supplier selection

    QSR and ISO requirements for supplier assessment.

    Recommended processes for new supplier qualification in a cost efficient manner.

    Who Will Benefit:

    Supply chain management

    Purchasing management

    Regulatory management

    QA management

    Executive Management

    Speaker Profile:

    Jeff Kasoff, RAC, is the Director of Quality at Byrne Medical, a leading manufacturer of endoscopy and colonoscopy devices, where he oversees the operation of the quality system. In this position, Jeff is responsible for oversight of the document control system, including maintenance of regulatory documentation. Prior to this, Jeff spent 13 years at Life-Tech, Inc. as the Director of Regulatory Affairs, where he was responsible for compliance of the corporate quality system. Jeff received his regulatory affairs certification in 1996.

    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.