VIEWS: 109 PAGES: 2 CATEGORY: Healthcare & Medicine POSTED ON: 12/7/2012
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.
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 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 Livermore Common, Fremont, CA 94539, USA Phone: 800-447-9407 or Fax your PO to: 302-288-6884 If you do not wish to receive this training alerts from GlobalCompliancePanel Click Unsubscribe
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