Medical Devices for Risk Management Techniques 2017
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Website http://www.compliance4all.com/control/w_product/~product_id=501425LIVE?channel=ourglocal_Aug_2017_SE |
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Category Risk Management Program, Medical Devices Webinars, FDA Expectations, Manufacturing Engineer trends, Regulatory Affairs, medical device industry, Stages of Risk Management, How to control those risks
Deadline: August 21, 2017 | Date: August 22, 2017
Venue/Country: Online, U.S.A
Updated: 2017-06-15 15:16:35 (GMT+9)
Call For Papers - CFP
Overview:This course will help you understand the regulatory requirements, including ISO14971, and how to create processes and procedures to implement them. Why should you Attend:Many companies have even experienced class action law suits because of product quality issues. An effective program of risk management can help you proactively identify and mitigate product risks.Areas Covered in the Session:Overview of the ISO14971 standard as it applies to medical device companiesIntegrating the new standard with ISO 13485 as part of your overall QMSConducting a review of the intended use of your deviceStages of Risk Management as well as Tools and TechniquesJudging the probability that harm may occur from those hazardsWho Will Benefit:Design EngineerManufacturing EngineerQuality EngineerR&D PersonnelR&D Project ManagersQuality ManagersAuditorsRegulatory Affairs SpecialistR&D ManagerSpeaker Profile:Susanne Manz MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities.Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: supportcompliance4All.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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