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    Record Retention Schedules in Support of Regulatory Compliance - Webinar by GlobalCompliancePanel

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    Website http://bit.ly/14icUfu | Want to Edit it Edit Freely

    Category Webinar, Health, Medical, Pharma, Clinical

    Deadline: September 04, 2013 | Date: September 04, 2013

    Venue/Country: USA, U.S.A

    Updated: 2013-08-12 15:32:36 (GMT+9)

    Call For Papers - CFP

    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.

    Why should you attend: The regulatory agencies drafted record retentions mostly to assure public safety. Organizations need to consider the value and liability of information independently of government requirements. Records and information could have value in generating future business profits and conversely could be a liability in the event of litigation.

    There is a perception that electronic information storage hardware is becoming less and less expensive. This view is correct, however, the expenditure of maintenance resources to support long term storage is much greater than expected because of rapid changes in technology. Saving most records indefinitely is a poor business practice not only because of unexpected costs but because there is increased risk of losing records that are essential to the business.

    Areas Covered in the Session:

    FDA and global agency records retention requirements

    Business records needs

    Business records liabilities

    Long term record preservation strategies

    Who Will Benefit:

    Research & Development

    QA

    QC

    Regulatory

    Clinical Operations

    Manufacturing

    Records Management

    Legal

    Information Technology

    Validation

    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.

    NetZealous LLC,

    DBA GlobalCompliancePanel

    161 Mission Falls Lane,

    Suite 216, Fremont, CA 94539, USA

    USA Phone:800-447-9407

    Fax: 302-288-6884

    webinarsatglobalcompliancepanel.com

    http://www.globalcompliancepanel.com

    Event Link - http://bit.ly/14icUfu

    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.