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Ensure process and product quality meet standards Certificate of fitness is a requirement Please note that if you have not received a response within 14 days of submitting your application that your application was unsuccessful. However, please keep a lookout on our website, [URL Removed] for available positions which may be inline with your career aspirations.
How To Navigate Clinical Data Per EU MDR By Matthias Fink, MD, TÜV SÜD America In May 2017, the European Medical Devices Regulation (MDR) 2017/745 was published to replace the current Medical Device Directive (MDD) and the Active Implantable Medical Device Directive (AIMDD). In April 2020, the European Parliament adopted the European Commission’s proposal to postpone the Date of Application (DoA) of the MDR by one year, and as such, the new DoA is May 26, 2021. It is worth noting that the end of the transition period for MDD and AIMDD certificates remains May 26, 2024, thus reducing the t...
Vietnam recently approved the fourth protocol amending the ASEAN Comprehensive Investment Agreement further building on its free trade environment
PAXXUS’ patented Chameleon technology is now available for use with uncoated Tyvek .
PDF, 962KB, 33 pages). 1. Summary Part of the MHRA’s role is the regulation of medical devices, including overseeing investigations into adverse events and promoting the safe use of devices in the UK. The MHRA continues to receive reports of incidents relating to bed rails and associated equipment. These incidents are concerning as some have led to patient harm or death, primarily from entrapment. This publication has been updated to reflect changes in devices and practices, as well as information gained from the investigation of adverse incidents. Who this guidance is for: This document is...