Record Retention Schedules in Support of Regulatory Compliance from GlobalCOmpliancePanel

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					                                                                       Toll Free Number: 800-447-9407


                                                                        RAPS Approved Webinar on


Record Retention Schedules in Support of Regulatory Compliance

Date: Wednesday, December 19, 2012                                      Time: 10:00 AM PST | 01:00 PM EST


Course "Record Retention Schedules in Support of        Duration:               60 Minutes
Regulatory Compliance" has been pre-approved by
                                                        Instructor:             Dr. Charlie Sodano
RAPS as eligible for up to 1.00 credits towards a
participant's RAC recertification upon full completion. Location:               Online


                    Dr. Charlie Sodano
                    Information Manager,                                    Register Now
                    eOrganizedWorld

Dr. Charlie Sodano Dr. Charlie Sodano is an experienced, globally recognized information management
professional. He began his career as a discovery research chemist at Pfizer and since 1985 has specialized in
the management of electronic as well as paper based records and information.     ...more

Overview:
Governmental record retention requirements during the life cycle of a drug will be discussed.
Particular attention will be focused on the scope of records that should be included in a retention
category. GLP, GMP, GCP and well as IND, NDA and BLA record retention requirements will be
compared to business needs.


Long term record preservation strategies based on global practices will be explored with an
emphasis on anticipated environmental changes.

Areas Covered in the Session:

    l   FDA and global agency records retention
        requirements
    l   Business records needs
    l   Business records liabilities
    l   Long term record preservation strategies



Who Will Benefit:

    l   Research & Development             Suggest a Topic
    l   QA
                                           More Webinars
    l   QC
    l   Regulatory
    l   Clinical Operations
    l   Manufacturing
    l   Records Management                 Click here to
    l   Legal
                                         register for this
    l   Information Technology
    l   Validation                            webinar


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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www.globalcompliancepanel.com
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CA 94539, USA

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DOCUMENT INFO
Description: Governmental record retention requirements during the life cycle of a drug will be discussed. Particular attention will be focused on the scope of records that should be included in a retention category. GLP, GMP, GCP and well as IND, NDA and BLA record retention requirements will be compared to business needs. Long term record preservation strategies based on global practices will be explored with an emphasis on anticipated environmental changes.