With the deadline of the MDR approaching, many medical device manufactures are scrambling to perform the necessary tests and evaluations that are required from the update. This has strained supplier resources and exposed a lack of expertise in the industry. This panel will discuss:
• The impact of the MDR on testing resources in the industry
• What tricks or direction has been taken to make sure devices are ready for their MDR submissions
• What testing has been needed and what outsourced expertise was used
• The experience of going through the MDR process and leanings that were developed.