Modular Medical (MODD) announced that BSI Group will serve as the notified body for the European regulatory clearance process. Unlike the U.S.

announced that BSI Group will serve as the notified body for the European regulatory clearance process. Unlike the U.S. process, European Union ("E.U.") clearance of a medical device is driven by ...

announced that BSI Group will serve as the notified body for the European regulatory clearance process. Unlike the U.S. process, European Union ("E.U.") clearance of a medical device is driven by a ...

Engaged BSI Group to start the process of obtaining regulatory clearance of the MODD1, next-generation insulin pump for the European market- Targeting Q1 2026 for expected clearance of the MODD1 in th ...

Innovative Health Sciences has successfully secured the exclusive Medical Device Regulations Quality Management System Certificate from BSI (CE MDR QMS), a leading notified body, thus facilitating ...

The Company successfully completed Stage I and Stage II Assessments performed by the notified body, BSI ... of medical devices. It builds on the ISO 9001 standard with additional regulatory ...

Image Analysis Group (IAG), a leading imaging Clinical Research Organization (iCRO), today announced the release of their ...

The Lumina submission was prepared in compliance with the EU Medical Device Regulation (MDR) and submitted to BSI Group, LifeSprout's Notified Body. Qi Liu, LifeSprout's Quality Director ...