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Good Laboratory Practice Regulations - Introduction and Strategies for Implementation - Webinar By GlobalCompliancePanel

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Good Laboratory Practice Regulations - Introduction and Strategies for Implementation - Webinar By GlobalCompliancePanel Powered By Docstoc
					                                                                                   Phone: 800-447-9407


                                                                      RAPS Approved Webinar on


Good Laboratory Practice Regulations - Introduction and Strategies for
Implementation

Date: Thursday, October 25, 2012                                     Time: 10:00 AM PDT | 01:00 PM EDT

Course "Good Laboratory Practice Regulations -                   Duration: 75 Minutes
Introduction and Strategies for Implementation" has
                                                                Instructor: Dr. Ludwig Huber
been pre-approved by RAPS as eligible for up to 1.25
                                                                  Location: Online
credits towards a participant's RAC recertification
upon full completion.                                                Price : $245.00 (for one participant)


                 Dr. Ludwig Huber
                 Chief Advisor - Global FDA                              Register Now
                 compliance, Agilent Technologies

Ludwig Huber, Ph.D., is Director of Labcompliance and Chief Advisor for global FDA compliance at Agilent
Technologies. He is the editor of Labcompliance, the global on-line resource for validation and compliance
issues for laboratories. ...more


Overview:
Analyzing biological fluids is one on the most difficult tasks in analytical laboratories. Most
challenging are interferences from matrices and decomposition products combined with low
concentrations of analyte. Correct validation of bioanalytical methods according to recent FDA and
industry recommendations ensures reliability, consistency and accuracy of bioanalytical data. But
because of the difficult nature of the analysis there are many questions. This seminar will
demonstrate how to validate bioanalytical methods and procedures for FDA compliance.

Complying with GLP regulations can increase the cost of a laboratory up to 30%. Companies or
employees either don't know exactly what GLP really means, what procedures are required and
how to implement GLP regulations.


Areas Covered in the Session:

    l   FDA and International GLP regulations: 21 CFR Part
        58, OECD
    l   Objectives and concepts of GLP's
    l   Special organizational requirements
    l   Responsibilities: Management, Study director, QA,
        analysts
    l   SOP requirements: type, formats and enforcement
    l   GLP studies: preparation, conduct, documentation
    l   Key requirements for equipment, facilities reference
        material, people
    l   Data generation and evaluation: raw data,
        intermediate results, final results
    l   Records keeping: format, length of time, archiving
        and reprocessing
    l   Preparing for FDA inspections



Who Will Benefit:

    l   Laboratory managers and          Suggest a Topic
        supervisors
    l   GLP auditors                      More Webinars
    l   GLP study directors
    l   QA/QC managers and
        personnel
    l   Analysts and other
        laboratory staff                  Click here to
    l   Regulatory affairs              register for this
    l   Training departments                 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
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:9/25/2012
language:English
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Description: Analyzing biological fluids is one on the most difficult tasks in analytical laboratories. Most challenging are interferences from matrices and decomposition products combined with low concentrations of analyte.