View all newsletters
Receive our newsletter - data, insights and analysis delivered to you
Sponsored by NSF International, Medical Devices

General Safety and Performance Requirements

Free White Paper

General Safety and Performance Requirements

By NSF International, Medical Devices

General Safety and Performance Requirements

By NSF International, Medical Devices
Enter your details to receive the free paper:

The heart of the European Union (EU) regulation of in vitro diagnostic medical devices (IVDs) lies in allowing market access to IVDs that offer clinical benefit, and are safe to the patient, the user of the IVD and others (such as service technicians).

The regulation is written so that requirements ensuring a high level of protection of health and safety are, where appropriate, must be fulfilled.

Under the EU IVD Directive 98 /79 / EC, manufacturers have been required to comply with the essential requirements (ERs).

NEWSLETTER Sign up Tick the boxes of the newsletters you would like to receive. The top stories of the day delivered to you every weekday. A weekly roundup of the latest news and analysis, sent every Friday. The medical device industry's most comprehensive news and information delivered every month.
I consent to GlobalData UK Limited collecting my details provided via this form in accordance with the Privacy Policy
SUBSCRIBED

THANK YOU

Thank you for subscribing to Medical Device Network