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Process Validation Principles and Protocols for Medical Devices - Webinar By GlobalCompliancePanel

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Process Validation Principles and Protocols for Medical Devices - Webinar By GlobalCompliancePanel Powered By Docstoc
					                                                                                      Phone: 800-447-9407


                                                                        RAPS Approved Webinar on


Process Validation Principles and Protocols for Medical Devices

Date: Thursday, November 15, 2012                                       Time: 10:00 AM PDT | 01:00 PM EDT


Course "Process Validation Principles and Protocols                 Duration: 60 Minutes
for Medical Devices" has been pre-approved by RAPS                Instructor: Jeff Kasoff
as eligible for up to 1.00 credits towards a                        Location: Online
participant's RAC recertification upon full completion.                Price : $245.00 (for one participant)


                      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. In this position, ...more


Overview:
The benefit of a consistent process is that the yield meets expected criteria. Firms that are able to
implement such processes minimize their process rejections and therefore maximize profit.


Domestic and international regulations actually assist in this endeavor, by setting forth the
requirements to assure a process is consistent, and that it yields output that is both safe and
effective. These requirements are applicable to both automated and manual processes. This
webinar explains the regulatory requirements for process validation, and also includes definitions
and application of applicable terminology, and hints and recommendation for the more common
types of process validation. Also covered will be the validation technique used for processes that
are already in place.


Areas Covered in the Session:

    l   What is Validation?
    l   When should it be used?
    l   How does it differ from verification?
    l   Validation vs. Verification: Which One?
    l   Protocol preparation
    l   Different types of validation
    l   IQ, OQ, and PQ



Who Will Benefit:

    l   Validation                          Suggest a Topic
        Specialists/Managers
    l   Process Engineers                   More Webinars
    l   Manufacturing Engineers
    l   Quality Engineers
    l   Product/Process
        Development personnel
    l   Research and Development            Click here to
        personnel                         register for this
    l   Quality/Regulatory                     webinar
        Personnel



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
GlobalCompliancePanel is an online knowledge fulfillment community portal & it has put together a new model
for online compliance training by creating a single window of learning opportunities for compliance
professionals & providing a forum for expert speakers/panelists to render their services through simplified
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
professionals can benefit from a wide range of training sessions, giving a diverse choice of events & all
sessions being either Live or recorded stream or in the form of audio CDs. GlobalCompliancePanel portal
ensures a secure & cost effective online environment and also support your E-learning and development
on/through our website. Keep track of all webinars arranged for your industry through notifications & event
calendars being mailed to your inbox. GlobalCompliancePanel opens new doors of learning opportunities for
professionals.


GlobalCompliancePanel
www.globalcompliancepanel.com
1000 N West Street Suite,
1200 Wilmington DE 19801

Phone: 800-447-9407 or
Fax your PO to: 302-288-6884
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DOCUMENT INFO
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posted:10/5/2012
language:English
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Description: The benefit of a consistent process is that the yield meets expected criteria. Firms that are able to implement such processes minimize their process rejections and therefore maximize profit.