Description

BSI hosts our 13th annual European Medical Device Roadshow for the medical device manufacturer regulatory affairs, quality assurance and related consulting community.

Join us again in person or for the virtual version of our Medical Device Roadshow exclusively focused on addressing European medical device regulatory and quality assurance requirements.

BSI will be sharing our current experiences, best practice and expectations from the perspective of the first notified body designated under the MDR (EU 2017/745). BSI The Netherlands (2797) is a leading Notified Body; we review medical devices to ensure that they conform to the requirements of the European Directives and Regulations. BSI UK (0086) is a UK Approved Body able to provide conformity assessments under the new UKCA scheme.

BSI’s medical devices consists of a team of over 1000 professionals including technical experts and internal clinicians competent in encompassing the full range of medical devices and management system standards. Our services include system certification to ISO 13485, CE marking, product testing, and standardization to support your global market access goals.

Our mission is to ensure patient safety while supporting timely market access to medical technology in a sustainable manner.

Register Now: https://cvent.me/3V8GND?RefId=MM