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Webinar: Enhancing Assay Sensitivity with Signal Amplification in a Microfluidic Assay
19 MARS 2026: Lyssna på vår gästtalare, Dr. Linda Klauss från Gyros Protein Technologies, när hon håller i ett exklusivt webbinarium där vi visar hur kombinatio...
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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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Upcoming training: MD software process design based on IEC 62304
Together with Intertek Academy, we offer a 2-day course in Stockholm, Sweden, covering Medical device software process design based on IEC 62304. This course is...
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QAdvis is now Aurevia
Two years ago, QAdvis became part of something bigger. At first, the change was mostly visible on paper — a new owner and later a new name: Aurevia. But this wa...
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Upcoming training: Cybersecurity standards for medical devices
This 1-day course on Cybersecurity standards for medical devices is designed to help professionals gain an understanding of the current standards within cyberse...
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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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ZEISS and EDGE leverage AI to transform bioimaging in the biopharma industry
Transforming complex bioimaging data to workflows offering actionable insights for decision-making to speed up drug discovery.
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Dive Into Current Metrology Trends
ZEISS INNOVATION TALKS - new video podcast series.
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Medicon Village breakfast seminar: ISO 10993-1 in practice
Don't miss our breakfast seminar at Medicon Village on May 28th: ISO 10993-1 in practice - connecting biological evaluation to your technical documentation.
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Upcoming training: Introduction to ISO 15189:2022
Do you work with quality management in a medical laboratory? Don’t miss our ISO 15189:2022 online training course on May 12-13th — designed to help you understa...
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Breakfast meeting in Norway: Essential Insights for Life Science Leaders on AI and Patient Journeys
We are pleased to invite you to an inspiring session with Niels Buch Leander, Chief Digital Officer at PharmaRelations.
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Any Image Size, Many Formats, AI-Powered
ZEISS arivis optimizes local server or cloud computation resources.
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Automated high-speed scanning of probes
ZEISS Axioscan 7 spatial biology.
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Meet Aurevia at the next Medicon Village Science for Breakfast
Join us for Science for Breakfast at Medicon Village on May 19th!
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Custom regulatory and clinical strategy workshops
A strong regulatory and clinical strategy early on can save months of rework later.
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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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Networking event in Denmark: Sponsor Oversight in Clinical Trials
We are excited to invite clinical trial professionals to a networking event to connect and discuss best practices, challenges and adaptive strategies in documen...
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Meet ZEISS at ELRIG Advances in Cell-based Screening 2026
Reserve your spot now.
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How MoniDose strengthened their regulatory confidence—fast
When MoniDose began their startup journey, regulations were their biggest challenge. Missing early design inputs tied to standards could have meant costly redesigns later.
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Important notification for IVDR Class C device manufacturers
Deadline for application is quickly approaching; 26 May 2026.
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Nordic collaboration delivering the next leap in spatial biology
Spatial biology is reshaping how researchers understand complex tissue environments, from tumour–immune interactions to treatment response. A major barrier has ...
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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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Supporting Investigator Initiated Clinical Studies—From Start to Finish
Many important clinical studies start with researchers – not pharmaceutical companies. In investigator initiated studies, pharmaceutical companies often support...
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Internal audits based on ISO 13485 for medtech organizations
Are you ready to turn your internal audits into real improvements? Internal auditing isn’t just about compliance—it’s a strategic tool for driving development a...
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