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    Best Practices for Lean Supplier Management in Compliance with FDA and ISO 13485 Requirements

    View: 133

    Website https://bit.ly/2qgYZYs | Want to Edit it Edit Freely

    Category FDA Medical Device Regulation; FDA Compliance

    Deadline: April 25, 2018 | Date: April 25, 2018

    Venue/Country: Training Doyens 26468 E Walker Dr,Aurora, Colora, U.S.A

    Updated: 2018-04-09 19:59:45 (GMT+9)

    Call For Papers - CFP

    OVERVIEW

    Notified bodies and the FDA cannot require your suppliers to meet the quality system regulations, so they must make sure you are exercising sufficient control over those suppliers. You must make sure your supplier management and system meets all required regulations, especially for critical suppliers. Sure, you depend on your suppliers to provide you with goods and services, but can your system prove that you have sufficient control over your suppliers to assure auditors and regulatory agencies that your product is safe and meets all your requirements? Your supplier management program can be in compliance, but is it cost effective? If not, your unquantifiable overhead costs may be out of control.Is your supplier management program collaborative with your suppliers? If your company is too demanding of your suppliers, you risk alienating them or even worse losing them – try explaining that to your supply chain management!

    WHY SHOULD YOU ATTEND

    This class will review the QSR and ISO requirements for supplier evaluation, including defining the types of suppliers that require evaluation, including “critical” suppliers and outsourced processes. The QSR and ISO requirements for supplier assessment will be defined as well. The webinar will discuss the application of a risk-based process resulting in a customized supplier management system.

    AREAS COVERED

    Review of FDA and ISO requirements

    Types of suppliers that must be qualified

    Defining critical suppliers

    Classification of suppliers

    Outsourced processes

    The Quality Agreement

    Recommended Practices

    LEARNING OBJECTIVES

    Review of FDA and ISO requirements

    Recommended Practices

    How to avoid “Death by Supplier Audit”

    Documentation requirements

    WHO WILL BENEFIT

    This webinar will provide valuable assistance to all regulated companies that are interested in implementing and maintaining a supplier management program that is both compliant and cost-efficient. The employees who will benefit include:

    Supply chain management

    Buyers

    Purchasing management

    CAPA Coordinators

    Regulatory management

    QA management

    Executive management

    Internal auditors

    SPEAKER

    Jeff Kasoff, RAC, CMQ/OE, LBB, has more than 30 years in Quality and Regulatory management. Over that time, Jeff has implemented and overseen quality system operations and assured compliance, at all sizes of company, from start-up to more than $100 million in revenue. This multi-faceted experience makes Jeff uniquely qualified to address compliance issues across the entire range of company sizes.

    For more detail please click on this below link:

    https://bit.ly/2qgYZYs

    Email: supportattrainingdoyens.com

    Toll Free: +1-888-300-8494

    Tel: +1-720-996-1616

    Fax: +1-888-909-1882


    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.