Control Change in Medical Device Engineering - 2017
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Website http://www.compliance4all.com/control/w_product/~product_id=501364LIVE?channel=ourglocal_Jul_2017_SE |
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Category Medical Device Engineering, Health Webinars, Production Management, medical device engineering courses, medical device engineering conference, medical device engineering courses, medical device engineering programs
Deadline: July 26, 2017 | Date: July 27, 2017
Venue/Country: Online, U.S.A
Updated: 2017-05-16 20:31:33 (GMT+9)
Call For Papers - CFP
Overview: This webinar will describe a system, based on the regulations and practical experience that will allow for efficient control of the change process. It will be compliant but not cumbersome or overly time consuming.Why should you Attend: FDA and ISO call for change control but do not provide any further guidance as to how to create a compliant system. The situation gets complicated when a company has suppliers or contract manufacturers and changes and approvals must pass from one to the other. Areas Covered in the Session:Change control procedurePre release and post release change controlChange transfer between company and suppliersForms and SOP'sWho Will Benefit:Development EngineersProduction ManagementQA/ QC PersonnelEngineering ManagementRegulatory PersonnelSpeaker Profile:Edwin Waldbusser is a consultant retired from industry after 20 years in management of development of medical devices (5 patents). He has been consulting in the US and internationally in the areas of design control, risk analysis and software validation for the past 8 years. Mr. Waldbusser has a BS in Mechanical Engineering and an MBA. He is a Lloyds of London certified ISO 9000 Lead Auditor and a member of the Thomson Reuters Expert Witness network.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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