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Webinar: Implications of the new Medical Device Regulation (MDR) from a product testing and certification perspective

Make sure you secure expert information on the new MDR in our Webinar on Thursday, Dec 1, 2016, 5pm CET.

Topic: Implications of the new...

Overview

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Make sure you secure expert information on the new MDR in our Webinar on Thursday, Dec 1, 2016, 5pm CET.

  • Topic: Implications of the new Medical Device Regulation (MDR) from a
    product testing and certification perspective
  • Date:  Thursday Dec 1, 2016
  • Time:  5pm CET
  • Duration: 60min
  • Language: English
  • Costs: Free of charge
  • Content: This webinar will introduce you to the changes of the new MDR and how they will impact your product research, design and development through to placing your product on the European market.

Register Now!

Medical device manufacturers face new challenges when trying to access the European market. Reason for this is the recent publication of the new Medical Device Regulation (MDR). The MDR will have a significant impact on clinical, preclinical and biocompatibility performance as well as other technical requirements.

Register for our Webinar on

„Implications of the new Medical Device Regulation (MDR)
from a product testing and certification perspective“

Thursday, Dec 1, 2016, 5pm CET

The new regulation will bring about significant changes for your business and it’s important to understand the implications early and start planning your transition immediately.

Register Now!

About the Strategic Alliance of CSA Group and BSI:

The alliance between CSA Group as one of the world’s leading medical device testing and certification organizations and BSI, one of the leading Notified Bodies in Europe, brings together an unrivaled mix of expertise, enabling you to create and bring your medical devices to patients and healthcare professionals all over the world — FAST and PREDICTABLY.

We understand that speed and certainty about project deadlines is paramount when accessing global markets. Therefore, our one-stop service guides electro-medical device manufacturers through the key stages of market access:

  • Product Testing according to IEC 60601
  • CE-Marking incl. Technical File Review
  • Quality Management System Assessment according to ISO 13485

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Event Details

December 1, 2016

Canada, China, Germany, Hong Kong, India, Italy, Japan, Korea, Netherlands, Singapore, Switzerland, Taiwan, Turkey, United Kingdom, United States

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