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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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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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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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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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ISO 20417 has been updated – what device manufacturers should consider
The new edition of ISO 20417 has been published, further clarifying expectations for information supplied with medical devices. Although not yet harmonized, the...
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Are you prepared for the updated ISO 10993 1:2025?
The latest edition of ISO 10993-1 reinforces the integration of biological evaluation with risk management, introduces updated approaches to exposure assessment...
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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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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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How Microscopy Can Help Families Grow
Advanced microscopy solutions can help bypass challenges and natural barriers of conception.
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