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Taking Advantage of the New EU MDR PMS Requirements

As part of MedTech Digital Week, Executive vice-president Oliver Christ and senior consultant of regulatory affairs and project management Berkin Guler at NSF’s PROSYSTEM discusses taking advantage of the EU Medical Devices Regulation (MDR) post-market surveillance (PMS).

As part of MedTech Digital Week, Executive vice-president Oliver Christ and senior consultant of regulatory affairs and project management Berkin Guler at NSF’s PROSYSTEM discusses taking advantage of the EU Medical Devices Regulation (MDR) post-market surveillance (PMS).

People are generally happy sticking to what they know, to their tried and tested habits as it is easy and painless.
COPQ is increasingly valuable for the pharmaceutical and medical device industries, where maximising product quality is paramount and defect reduction has an additional knock-on effect.
Deciding to use a CMO requires a thorough due diligence exercise conducted both as desktop and on-site reviews.
"Planned" shutdown maintenance is vital for any production facility.
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