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IVDR Reality Check: Are We Moving Fast Enough?
As of February 2025, around 1,500 IVDR certificates have been issued. But if an estimated 18,700 devices still need certification before the 2029 deadline, then...
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Scale Up Your Image Analysis
ZEISS arivis Hub for accelerated analysis and faster results.
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Introducing ZEISS arivis Pro 4.2
Your solution for advanced image analysis and visualization.
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The Future of Metrology is Coming to Your Region
Join our event series.
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Meet us at Control 2025
Innovations that drive efficiency.
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Integrated solutions for liquid handling
Greater efficiency for manufacturers in laboratory automation and many other industries
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ZEISS Quality Innovations at CONTROL
May 6-9, 2025 in Stuttgart.
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Reduced heat transfer to the media with media-separated valves
In laboratory automation, many liquids are used that react sensitively to heat. One possible factor for the transfer of heat to the fluid are media-separated so...
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ZEISS Connected Quality: One metrology hub
The new product family ZEISS CONNECTED QUALITY is the solution for quick and secure data exchange, quality management and efficient system monitoring.
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Organize and Manage Digital Classrooms
Create engaging lessons with ZEISS Labscope Teacher.
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New version of ISO 10993-1: the core standard for the biological evaluation of medical devices
ISO 10993-1, the core standard for the biological evaluation of medical devices, has been under revision over the past few years. A Final Draft International St...
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Enhance your expertise with your measuring software
Discover the training options in our ZEISS Metrology Portal.
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Could an overly burdensome QMS be the organization’s own doing?
Although the above statement is intentionally somewhat provocative, it does hold a degree of truth. Organizations that are generally negative toward regulations...
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Will the FDA’s new transparency policy extend to medical devices? (Part 1)
In a significant policy shift, the FDA has begun publishing Complete Response Letters (CRLs) for drug and biologic applications that were initially rejected but...
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Explore our tailored program for Control 2025
Choose an innovation tour, or join our industry-specific guided tours.
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FDA’s new CSA guidance: transforming software validation for production and quality systems
FDA’s final guidance on Computer Software Assurance (CSA) for Production and Quality System Software marks a significant modernization of software validation practices.
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The FDA’s new transparency policy (Part 3)
As transparency and consistency become increasingly emphasized by the FDA, medical device manufacturers must approach their submissions with both thoroughness a...
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Discover ZEISS ZEN core – now for electron microscopy
Watch the recording of our free webinar.
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Nivågivare för skummande media
NSL-F-givarna från Anderson-Negele utmärker sig särskilt genom den säkra funktionen, även vid användning av starkt vidhäftande och skummande medier. På så sätt ...
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The FDA’s new transparency policy (Part 2)
In the second part of our article series on the FDA’s new “radical transparency” initiative, we explore regulatory strategies to navigate the potential impact o...
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ZEISS at EMO Hannover 2025
Experience some of the most exciting highlights from our ZEISS product portfolio.
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New Insights into Microscopy
Watch the recording of our free webinar.
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Webinar: Automate your processes
Free ZEISS webinar on January 30th, 2025.
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Discover the new ZEISS Axioscan 7 clinical
Your digital slide scanner for diagnostics & clinical research.
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