Fritextsökning
Innehållstyper
-
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...
-
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...
-
The Versatile Solution for Quality Management and Data Analysis
Join our ZEISS PiWeb webinar on March 26.
-
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...
-
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...
-
How Microscopy Can Help Families Grow
Advanced microscopy solutions can help bypass challenges and natural barriers of conception.
-
Multiplex Immunofluorescence
New protocol for efficient generation of seven-color, whole slide imaging with ZEISS Axioscan.
-
Insurance in Life Science: From risk to resilience
Are you visiting The Future of Swedish & Danish Life Science event in Lund 23 April? Don't miss the Gallagher seminar on Risk and Insurance in the Life Sciences sector.
-
Transport validation for medical devices
According to MDR 2017/745, “Devices shall be designed and manufactured in such a way as to ensure that their characteristics and performance during their intend...
-
ZEISS Quality Innovations Worldwide
All events now in one video.
-
Enhancing Spatial Biology
Enabling easy, reproducible multiplex spatial profiling at scale.
-
Breakthrough devices: Key insights from MDCG 2025-9 guidance
The Medical Device Coordination Group (MDCG) has published guidance MDCG 2025-9 to streamline the pathway for breakthrough devices (BtX) under the EU Medical De...
-
Precision, balance and clinical experience
Phase II is often the most crucial phase of clinical development. This is where the study design is validated in practice, effect must be demonstrated, and wher...
-
Season 2 of ZEISS Metrology Expert Tips is now live
Experts from season 1 compete against each other in #measuringhero quiz.
-
The Beauty of Clinical Microscopy of Urine Sediment
Read about concrete observations using phase contrast and polarized light.
-
From Image to Results
3D multiplexing spatial omics workflows in neuroscience.
-
Webinar: Imaging of Complex In-Vitro Models
Deep Imaging and Scalable Analysis of Hepatic Spheroids with ZEISS LSM 910/990 Lightfield 4D.
-
Optical inspection made easy
New ZEISS Smartzoom 100 product video.
-
Shaping the Future of Metrology – Live in Your Region
Insights into our event series.
-
PMS, Vigilance and Risk Management
Post-Market Surveillance (PMS) is more than complaint handling – it’s a strategic tool for patient safety, regulatory compliance, and continuous improvement. Un...
-
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...
-
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...
-
Integrated solutions for liquid handling
Greater efficiency for manufacturers in laboratory automation and many other industries
-
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.
BREAKING