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Webinar on Medical Device Classifications

Start Date:
Friday, 6 May, 2016
End Date:
Friday, 6 May, 2016 2:00pm
Internal Medicine, Physical Medicine, Business Practice, Health & Nutrition

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 Department Product Design and Development Departments


5939 Candlebrook Ct,
ON L5V 2V5,

Organizer Details

Conference organized by Compliance Trainings

This new 2-day Seminar on Computer Systems Validation will explore proven techniques for reducing costs associated with implementing, using, & maintaining computer systems in regulated environments. The FDA performs GxP & Part 11 inspections, with an updated Annex 11 regulation, & companies must update their systems and processes to maintain compliance.

861, Peripheral Road, Koramangala, Bangalore

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