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Classifying Medical Devices - US and EU 2017
21 Mar 2017
Webinar
Home
Classifying Medical Devices - US and EU 2017
Description
Topics
Medical device determination
Purpose and reason for classifying medical devices
Medical Device exemptions and when they apply
The medical device classification panels
The process of classifying a medical device in the US
Product code classification database and how it is used
The impact of the new EU Medical Device Regulation on EU medical device classifications
The process of classifying a medical device in the EU
Who should Attend
Audit and Compliance Personnel
Medical Device industry
Quality Professionals
Regulatory Professionals
Design Engineers
Risk Managers
VP, Directors and Managers of medical device design functions
Research and Development Engineers
Medical device marketing and sales personnel
Past Events
Classifying Medical Devices - US and EU 2017 - 21 Mar 2017, Webinar
(66240)
Important
Please, check "Classifying Medical Devices - US and EU" official website for possible changes, before making any traveling arrangements
Event Categories
Business:
E-Business, Finance, Innovations, Internal Audit & Compliance, Marketing & Sales, Quality assurance
Education:
E-learning
Health & Medicine:
Medical device, Medical laboratories, Medical technology
Technology:
Data management
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