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Innehållstyper
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Experience fast and easy optical inspection
Webinar recording: ZEISS Smartzoom 100.
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Strengthen your team with Clinical and Regulatory Experts
Not every challenge calls for a permanent hire.
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Clinical and regulatory expertise that delivers results
Organizations in the life sciences sector are under constant pressure to meet regulatory requirements, maintain clinical study timelines, and ensure inspection ...
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Medtech Compliance Forum by Aurevia & RAPS
We are excited to announce that registration is now open for the Medtech Compliance Forum by Aurevia & RAPS, taking place as part of Labquality Days 2027 in Helsinki, Finland.
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Experienced clinical and regulatory support for a busy autumn
The post-summer backlog is real.
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Expanding into the EU market?
Expanding into the EU market as a medical device or IVD manufacturer? For non-EU/EEA companies, appointing a European Authorised Representative (EAR) is not jus...
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Flexible clinical research support for your urgent project needs
When resources are stretched or timelines are tight, waiting is not an option.
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Streamline medical device development with an integrated platform
Developing medical devices (MD) today means navigating complexity—regulatory requirements, documentation, risk management, and fast-moving innovation. What if y...
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Imaging Core Lab and Clinical Adjudication in Clinical Studies
At Aurevia, we offer centralized adjudication and core lab services where experienced clinical experts, in close collaboration with our project managers, ensure...
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Keep projects on track this autumn with Senior Clinical and Regulatory Expertise
Where could senior clinical and regulatory expertise make the biggest impact this autumn?
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UK Responsible Person: A critical partner for UK market access
If you're a non-UK manufacturer, appointing a UK Responsible Person (UKRP) is mandatory for placing medical devices and IVDs on the UK market.
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First Patient Enrolled in International Phase III Clinical Trial
We are proud to announce that the first patient has been enrolled in an international Phase III clinical trial investigating a treatment for bacterial vaginosis.
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WEBINAR | Mastering Regulatory Affairs across the Nordics
This webinar is for you who work in Regulatory Affairs but only focus on one Nordic market today and are curious to learn more about the requirements across the Nordic region.
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Customer success stories: Advancing quality, regulatory and clinical research excellence
Strong partnerships drive successful outcomes.
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Explore the ZEISS Innovation Summit 2026
Centered around the theme “Turning Insights into Impact,” the event brings together international executives, leaders, scientists, and innovators from leading c...
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ZEISS is a partner of the 75th Lindau Nobel Laureate Meeting
The partnership underscores ZEISS' commitment to research, innovation, and the dialogue between science and industry.
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Rostfria kopplingar för krävande miljöer
När driftssäkerhet och korrosionsskydd är avgörande spelar valet av koppling en central roll. Genom OEM Automatic erbjuds Schwer Fittings rostfria klämringskopp...
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5 reasons to choose Aurevia as your quality, regulatory and clinical research partner
In today’s complex life sciences landscape, success depends on working with a partner who understands both the regulatory environment and the realities of clinical research.
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New ZEISS microscopy customer portal
Faster access, better organization, and a simpler way to stay in control.
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Ystral inviger nytt testcenter för processutveckling
Ystral har öppnat ett nytt testcenter vid huvudkontoret i Ballrechten-Dottingen, Tyskland. Anläggningen stärker företagets möjligheter att genomföra fler kundte...
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Medtech Compliance Forum by Aurevia & RAPS - part of Labquality Days
Aurevia is pleased to announce a new partnership with RAPS, the Regulatory Affairs Professionals Society, to strengthen the medtech programme at Labquality Days...
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ZEISS announces strategic collaboration with Envision Health Technologies to advance glaucoma care
ZEISS Medical Technology and Envision Health Technologies will collaborate to advance the next generation of patient-accessible, software-driven visual function...
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Flexibel tryckmätning för krävande processer
OEM Automatic erbjuder processtryckgivare i serie IPT-20 / IPT-21 från WIKA – en robust lösning utvecklad för att möta behoven i en mängd olika industrier. Med ...
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How ZEISS/RAITH Solutions Enable High Quality Nanopatterning & Nanolithography
Join our Webinar on 2nd July 2026.
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