How to Conduct a Hazard Analysis/Risk Assessment
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Category Seminar, Health, Medical, Pharma, Clinical
Deadline: July 22, 2014 | Date: July 22, 2014
Venue/Country: USA, U.S.A
Updated: 2014-05-28 17:48:33 (GMT+9)
Call For Papers - CFP
Overview:This interactive webinar teaches how to determine and document risk in a process in order to reduce validation time and ensure compliance.What makes this session unique are the real life examples that make application of the techniques understandable in the context of any validation project. It includes a workshop for participants to perform their own hazard analysis so they are proficient in apply the risk-based techniques. Areas Covered in the Session:Interactive real life examples.How to identify risk and establish mitigations.How to use the hazard analysis to make validation efficient. How to document the risk assessment using a templateHow risk assessment reduces validation time.Determine risk in a process to reduce the testing effort. Traceability made automaticWorkshop exercises.Who Will Benefit:All system usersITQAQCLaboratory staffManagersExecutivesQuick Contact:GlobalCompliancePanel USA Phone:800-447-9407Fax: 302-288-6884webinarsglobalcompliancepanel.comhttp://www.globalcompliancepanel.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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