VIEWS: 45 PAGES: 2 CATEGORY: Hospital POSTED ON: 9/25/2012
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.
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 If you do not wish to receive this training alerts from GlobalCompliancePanel Click Unsubscribe
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