Webinar on Medical Device Classifications
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Website https://compliancetrainings.com/product/medical-device-classifications/ |
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Category FDA Compliance, Medical Devices
Deadline: January 13, 2017 | Date: January 13, 2017
Venue/Country: o, Canada
Updated: 2016-12-19 22:43:41 (GMT+9)
Call For Papers - CFP
Description:When designing and developing medical devices it is essential to properly classify your device early on in the process to prevent costly and cumbersome regulatory issues and added or unnecessary work later in the design and development process. The determination process, how you apply the process to your device, is complex and requires several levels of analysis to make the proper device classification.This workshop will provide insight into the classification process as regulated by the FDA and will provide a methodology to assist in properly making your classifications.Areas Covered in the Session :Medical Device classifications – an OverviewDoes the product emit radiation?Determining if your product is a medical deviceWhat are the medical device classification panels?What are exemptions and when do they apply – Class I/II?What is the product code classification database and how is it used?What is reclassification?Who Will Benefit:Quality EngineersProject ManagersRegulatory Affairs DepartmentProduct Design and Development Departments
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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