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UK – Overview of medical device industry and healthcare statistics
Below you will find basic demographic and economic data for the United Kingdom (UK), plus specific information about the country's medical device and
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CER Complience webinar EMERGO 2018
WATCH NOW: Ensure Your CER Complies with MEDDEV 2.7/1 v4
Since the publication of MEDDEV 2.7/1 rev4 and the Medical Devices Regulation (MDR), clinical data is under heavy scrutiny by Notified Bodies and
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Classification Borderline: What Constitutes a Medical Device?
Distinguishing a medical device from a cosmetic, biocide, or drug is complicated when a product seems to fit the definitions for two or more product
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Introduction to CE Marking for Medical Devices
Are you a medical device manufacturer with your eye on the European market? If so, you've probably heard the term "CE Mark". The CE Mark is the key
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Clinical Investigational Studies in Europe
Many medical device companies think they are ready to conduct clinical investigation studies when they are actually months--if not years--away from
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Learn about basic demographic and healthcare market data on the European Union
EUROPE – Overview of medical device industry and healthcare statistics
Below you will find basic demographic and healthcare market data on Europe, plus specific information about the medical device and healthcare
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Preparing to Change your European Notified Body
The transition deadline for the European Medical Devices Regulation (MDR 2017/745) will be here soon and medical device companies are preparing to
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Medical Device Labeling, Standards and Symbols
Selling your medical device in the global marketplace requires you to consider other languages and cultures. There are over 20 official languages in
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How to Select and Change a Notified Body in Europe
Selecting a Notified Body (NB) is an important (and required) step for obtaining CE Marking and registering your medical device for sale in the
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