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ZEISS Medical Days 2026: See all highlights in one compact recap video
The video offers impressions from presentations, live demonstrations and discussions.
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Integrated Clinical and Regulatory Support for Oncology Trials
Aurevia is a European Contract Research Organization (CRO) and regulatory partner supporting biotech, pharmaceutical, and medtech companies in the development a...
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CTIS updates strengthen compliance and transparency
The Clinical Trials Information System (CTIS) has introduced several updates aimed at improving safety reporting, communication, and regulatory compliance for sponsors.
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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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From diagnosis to treatment, ZEISS introduces innovations across ZEISS Retina Workflow
ZEISS Medical Technology advances its ZEISS Retina Workflow with digital and surgical enhancements, and new imaging technologies.
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Introducing ZEISS VersaXRM 5 Insight
Stay in the flow from overview to insight.
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On-demand webinar: ZEISS Lightfield 4D for high-content tumor microtissue screening
From reliable and scalable 3D models to quantitative insights.
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ZEISS elevates ophthalmic workflows at ESCRS with new surgical and digital advancements
ZEISS Medical Technology will showcase its latest portfolio advancements and workflow enhancements for cataract, corneal refractive, and retina, at the European...
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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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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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The Three Pillars of Clinical Evidence Under the IVDR — What Manufacturers Need to Know
The IVDR raises the bar. Many in vitro diagnostic (IVD) medical device manufacturers still underestimate how significantly the IVDR (EU) 2017/746 has raised the...
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Webinar – Is your AI software a medical device?
Join our free webinar on 29 October 2026, 13:00–13:45 CET, with Oscar He Lindholm, Client & Business Development Partner at GBA Key2Compliance. Oscar will expla...
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The IVDR Transition Is Not Over: Key Deadlines and Common Pitfalls
While the transitional periods have been extended through Regulation (EU) 2024/1860, the extension is not automatic. IVD manufacturers must meet specific interi...
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High-pressure technology takes nanoprocessing from the lab to pharmaceutical production
Controlling particle size is an important consideration in the development of biological medicines, vaccines and lipid nanoparticles. Microfluidics’ high-pressu...
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Master Medical Device Sterilization
The Essential 4-Day Training for Auditors, Assessors, and Quality Professionals
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Why are Aurevia and RAPS collaborating on the Medtech Compliance Forum?
We asked Mika Siitonen, Operations Manager, Digital Health at Aurevia, and the lead for the Medtech Compliance Forum, to explain the thinking behind the collabo...
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Experience fast and easy optical inspection
Webinar recording: ZEISS Smartzoom 100.
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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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New ZEISS microscopy customer portal
Faster access, better organization, and a simpler way to stay in control.
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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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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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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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EDIH Summit 2026 Finalist: Simplifying Regulatory Compliance
Excited to be recognized as one of five European Digital Innovation Hub (EDIH) Community Award finalists at the EDIH Summit 2026!
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Partner article: Building sponsor oversight for a pivotal Phase III program
OncoZenge is preparing to initiate a pivotal Phase III study for BupiZenge™, a treatment for oral mucositis pain in cancer patients. As the program advances int...
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