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Trelleborg helps wearables firms navigate new EU regulation The medical device tech firm is poised to assist manufacturers in navigating the new European Medical Device Regulation, which goes into effect this week. Navigating the global regulatory landscape can be confusing for anyone in the life-sciences realm, including manufacturers that make wearable sensors and other medical devices. To that end, Trelleborg Healthcare and Medical is offering manufacturers that supply such products to European clients resources (including a free webinar) geared toward helping them understand and comply with the Medical Device Regulation (MDR), which goes into effect May 26. The new MDR is intended to help protect patients from risks that may be posed by a range of medical products. Florance Veronelli, segment manager with Trelleborg Sealing Solutions, talked about the assistance offered by the firm, and what the regulation means for the industry.

Florance veronelliTrelleborg sealing solutionsTrelleborg healthcareMedical device regulationTrelleborg sealingMarkets amp regulationsClinical developmentMedical devicesRegulatory affairsEuropean unionDecentralized trialsட்ரெலெபோர்க் சீல் தீர்வுகள்ட்ரெலெபோர்க் சுகாதாரம்மருத்துவ சாதனம் ஒழுங்குமுறைட்ரெலெபோர்க் சீல்சந்தைகள் ஆம்ப் ஒழுங்குமுறைகள்