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SGS webinar on IVDR & MDR certification process
Are you supporting manufacturers in navigating the IVDR or MDR certification process? Join our complimentary online session designed specifically for consultanc...
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ZEISS debuts DORC EVA NEXUS for cataract surgery at ESCRS
Now spanning ZEISS Retina and Cataract Workflows, the EVA NEXUS™ ophthalmic surgical system from ZEISS comes in a cataract-only configuration, bringing a tailor...
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EVENT | As fewer and fewer new medicines reach Swedish patients – can Swedish life science...
Breakfast Event | September 30 | 8.00-10.00 | SWEDEN
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ZEISS CLINIC 360 receives FDA 510k clearance
The ZEISS CLINIC 360 all-in-one browser-based software solution aggregates clinical data at scale and powers advanced analytics for streamlined ophthalmic workf...
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OCTONIQ, Ett smart, modulärt CIP-system.
OCTONIQ, ett modulärt CIP-system från AxFlow Systems som effektivt rengör din anläggning med hög precision. Systemet minskar förbrukningen av både vatten, energ...
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ZEISS Innovation Summit returns to Berlin
Gain insights from experts for future-ready quality assurance.
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Cavidi Secures US Patent Allowance for BOLD Signal-Amplification Technology
The allowance protects Cavidi's Enzyme Enhanced ELISA invention in the US, five years after its first patent filing in Sweden.
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Ensuring Safety and Compliance for IVD Products
In vitro diagnostic medical devices (IVDs) play a crucial role in diagnosis and treatment, as a significant proportion of healthcare decisions are based on labo...
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Rätt ventil för rätt applikation – hitta lösningen hos OEM Automatic
Rätt ventil är avgörande för ett tillförlitligt flöde och en driftsäker process. OEM Automatic erbjuder ett brett sortiment av industriventiler för olika applik...
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What if some of the most influential systems in healthcare are the least regulated?
While MDR has placed high demands on medical device manufacturers, a new reality is emerging in healthcare. AI‑based triage tools, prioritization systems, and d...
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From regulatory requirements to clinical reality: putting clinical & performance evidence into focus
Clinical evidence remains one of the most challenging areas of medical device compliance. What do notified bodies expect? How can real-world and digital evidenc...
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AI in Medical Devices: Understanding the Review Process and Common Gaps
Join GBA Key2Compliance and BSI for a free webinar on 19 November 2026, 13:00–14:00 CET, exploring the regulatory review process for AI-enabled medical devices....
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Upcoming Course: Quality Management System according to EN ISO 13485:2016 - in practice
Do you work with medical devices? Understanding and implementing a robust Quality Management System (QMS) is key to regulatory success—and often a prerequisite for CE-marking.
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Smartare kvalitetskontroll med Zebra NS42 från OEM Automatic
OEM Automatic erbjuder Zebra NS42, en smartkamera med integrerad Smart Vision Sensor som kombinerar avancerat maskinseende med intelligent avvikelsedetektering....
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Effektiv flödesmätning för vatten- och avloppssystem med FLUXUS WD
OEM Automatic erbjuder Emersons ultraljudsflödesmätare Flexim FLUXUS F731WD och F532WD – två tillförlitliga lösningar för noggrann flödesmätning inom vatten- oc...
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QAdvis & Scandinavian CRO are now Aurevia
Two years ago, we became part of something bigger. At first, the change was mostly visible on paper — a new owner and later a new name: Aurevia.
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Pumphuvudkonfiguration: Optimera flöde och vakuumprestanda
Konfigurationen av en membranpumps pumphuvuden spelar en avgörande roll för att bestämma dess flöde, vakuumkapacitet och totala prestanda. Medan membranmekanism...
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From innovation to compliance: Medtech Compliance Forum by Aurevia & RAPS explores health technology
How do you ensure innovation keeps pace with regulation? AI, software as a medical device, lifecycle management, post-market monitoring, clinical evidence, and ...
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Your UKRP Partner for Medical Device Market Access in the UK
Entering the UK market requires more than just registration—it requires the right regulatory partner.
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Kostnadseffektiv och driftsäker nivåmätning med Rosemount 1208
OEM Automatic presenterar Rosemount 1208 – en kompakt och beröringsfri nivå- och flödesradar som kombinerar hög precision med enkel installation. Den 80 GHz-bas...
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Medical Device Software Process Design: Why IEC 62304 Matters
How confident are you that your medical device software processes could withstand a regulatory review?
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Kostnadseffektiv automation för framtidens företag
Medelstora företag möter idag flera utmaningar – stigande kostnader, hård konkurrens och förändrade kundkrav. För att kunna fortsätta växa och samtidigt behålla...
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Upcoming Course: Medical Device Software Process Design Based on IEC 62304
Do you work with medical device software process design? Together with Intertek Academy, we offer a 2-day course covering medical device software process design...
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Rätt nivåmätning för en säkrare och mer tillförlitlig process
Att välja rätt nivåmätning är viktigt för att säkerställa en stabil och driftsäker process. OEM Automatic erbjuder ett brett sortiment av nivågivare, nivåvakter...
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