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Supplier Evaluation and Assessment: How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner from GlobalCompliancePanel

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Supplier Evaluation and Assessment: How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner from GlobalCompliancePanel Powered By Docstoc
					                                                                       Toll Free Number: 800-447-9407


                                                                        RAPS Approved Webinar on


Supplier Evaluation and Assessment: How to Meet FDA QSR and ISO
13485 Requirements in a Cost-Effective Manner

Date: Thursday, December 20, 2012                                       Time: 10:00 AM PST | 01:00 PM EST

Course "Supplier Evaluation and Assessment: How to
Meet FDA QSR and ISO 13485 Requirements in a            Duration:               60 Minutes
Cost-Effective Manner" has been pre-approved by         Instructor:             Jeff Kasoff
RAPS as eligible for up to 1.00 credits towards a       Location:               Online
participant's RAC recertification upon full completion.


                      Jeff Kasoff
                      Director of Regulatory                                Register Now
                      Affairs, Life-Tech, Inc

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.     ...more

Overview:
Supplier qualification and assessment is required in both the QSR regulations and ISO standards.

Many companies spend a great deal of time and money in pursuit of compliance with this. Many
companies can spend MUCH LESS time and money, and still be in control of their suppliers and in
compliance with the regulations. This presentation will review the QSR and ISO requirements for
supplier evaluation and assessment, and provide cost efficient, equally compliant options to many
of the most common practices.



Areas Covered in the Session:

    l   Regulatory Requirements
    l   Key Elements of a Supplier Qualification Program
    l   Utilizing Quality Agreements
    l   Supplier Assessment
    l   Supplier Nonconformance
    l   Required Documentation



Who Will Benefit:
This webinar will provide
valuable assistance to all
regulated companies that are               Suggest a Topic
interested in incurring less cost
                                           More Webinars
on supplier evaluation and
assessment.
The employees who will benefit
include:
                                           Click here to
    l   Purchasing Management
                                         register for this
    l   Regulatory Management
    l   QA Management                         webinar
    l   Consultants



It would be really nice if you can circulate this mail to all your deserving colleagues who can
immensely benefit from this program.


For more information, please contact the event coordinator. We look forward to seeing you at the webinar.


Best regards,
Event-coordinator
GlobalCompliancePanel

About GlobalCompliancePanel
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for online compliance training by creating a single window of learning opportunities for compliance
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online training delivery mechanisms. Our commitment is give compliance regulatory training, showcasing of
best industry practices & quality enrichment training sessions in a most cost effective manner. Compliance
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www.globalcompliancepanel.com
Livermore Common, Fremont,
CA 94539, USA


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DOCUMENT INFO
Description: Supplier qualification and assessment is required in both the QSR regulations and ISO standards. Many companies spend a great deal of time and money in pursuit of compliance with this. Many companies can spend MUCH LESS time and money, and still be in control of their suppliers and in compliance with the regulations. This presentation will review the QSR and ISO requirements for supplier evaluation and assessment, and provide cost efficient, equally compliant options to many of the most common practices.