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Aurevia expert spotlight: 3 questions with our risk management expert
Meet Cristina Albu Barkman, Principal Consultant, and one of Aurevia’s most experienced specialists in medical device risk management. With more than 25 years i...
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Any Image Size, Many Formats, AI-Powered
ZEISS arivis optimizes local server or cloud computation resources.
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Why Data and AI Skills Are Becoming Critical in Life Science Teams
Life Science organizations are investing heavily in data platforms, digital tools and AI driven solutions. From production and quality to clinical development a...
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New global standard for clinical evaluation is on the horizon: ISO/DIS 18969
A new global standard for clinical evaluation is on the horizon: ISO/DIS 18969. The core message is straightforward: clinical evaluations should be seen as a pr...
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New ZEISS Crossbeam 750 FIB-SEM for high-accuracy sample preparation workflows
Advances in simultaneous SEM imaging while FIB milling provide unmatched feedback for precision endpointing.
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ZEISS Quality Innovations Worldwide
All events now in one video.
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The Versatile Solution for Quality Management and Data Analysis
Join our ZEISS PiWeb webinar on March 26.
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ISO 13485 Standard Internal Auditing Course
Do you work with medical devices and quality management? Strengthen your expertise with our ISO 13485 Standard Internal Auditing Training — designed to give you...
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How Microscopy Can Help Families Grow
Advanced microscopy solutions can help bypass challenges and natural barriers of conception.
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Clinical evaluation of class I medical devices
The Swedish Medtech Regulatory Summit is just around the corner — taking place on March 12th at Hilton Slussen in Stockholm. We’re proud to share that our Senio...
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Multiplex Immunofluorescence
New protocol for efficient generation of seven-color, whole slide imaging with ZEISS Axioscan.
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Clinical Evaluation in MedTech – Expert Insights from Sandra Sernbo for Building Safe Medical Device
The article highlights the role of clinical evaluations at GBA Key2Compliance in ensuring that medical devices are safe, effective, and ready for real-world cli...
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Internal audits – an opportunity to improve Medical Devices
Internal audits are more than an ISO 13485 requirement — they give medical-device companies a chance to improve product quality and processes. External auditors...
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Smooth Flow Pumps – A Milestone in Diaphragm Pump Innovation
From high-resolution printing to life-saving devices, our advanced flow technology delivers smooth, turbulence-free performance where precision is everything.
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Multiplex immunofluorescence chemistries with ZEISS tissue multiplexing workflow
Bringing leading multiplex immunofluorescence chemistries together in one automated 8-channel imaging platform.
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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 showcases comprehensive workflow for full spectrum of retina care at EURETINA
ZEISS Medical Technology combines its diagnostic, surgical and digital technologies to support healthcare professionals in advancing retinal care.
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ZEISS Smartzoom 100 for Inspection Efficiency
Catch up on our free webinar.
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Safety Data That Makes a Difference – Insights from Safety Manager Ida Björklund
The article highlights safety manager Ida Björklund’s approach to clinical trial safety. She emphasizes that all safety data, no matter how small, must be caref...
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Discover ZEISS ZEN core – now for electron microscopy
Watch the recording of our free webinar.
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One System, Three Contrasting Techniques
ZEISS Axioscan 7 clinical - your digital slide scanner for diagnostics and clinical research.
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Simplifying IVDR Compliance: Insights from Senior Consultant Emily Malmberg
Navigating the complex demands of the IVDR requires both strategic planning and deep regulatory insight. At GBA Key2Compliance, Senior Consultant Emily Malmberg...
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New Insights into Microscopy
Watch the recording of our free webinar.
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Why Less is More in Clinical Data – Insights from Senior Clinical Data Manager Åsa Testad
With a background in informatics and programming, Åsa Testad leads clinical data management at GBA Key2Compliance. She ensures that data in clinical studies is ...
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