The Netherlands Standardization Institute (NEN) has launched a free risk analysis tool to help healthcare organizations and other entities that process personal health data carry out the information security risk assessment required under NEN 7510.
The Dutch Accreditation Council (RvA) has completed iits 2025 peer evaluation by the European co-operation for Accreditation (EA), a review that determines whether it can remain a signatory to the EA Multilateral Agreement.
The Netherlands Standardization Institute (NEN) is inviting experts to join its Clinical Research standards committee to help shape international standards for clinical investigations of medical devices.
From February 1, 2026, NEN, the Netherlands’ national standards body, will supply its standards only in digital form, ending the sale of printed standards.
The Netherlands Standardization Institute (NEN) has opened a consultation asking Dutch stakeholders whether the water sampling standard NEN-EN-ISO 19458 should be revised, with input open until February 19, 2026.
Seven new management system standard packages are now available on NEN Connect, the online platform of NEN that provides digital access to standards and related tools.
The Netherlands Accreditation Council (RvA) has released a revised version of its Accreditation Specification ASR007, which sets the requirements for conformity assessment schemes and the organizations that manage them.
The Netherlands Standardization Institute (NEN) has set the initial scope for developing a new Dutch Practice Guideline (NPR) on sustainability in medical devices.
The Dutch In Vitro Diagnostics Standards Committee is driving a wide range of international work on new laboratory and diagnostic standards, reflecting the rapid rise of digital tools, artificial intelligence, and smarter testing systems.
The Netherlands Standardization Institute (NEN) has released NPR 5333:2025, a new guideline that helps organizations maintain control over agile-style IT development.
The International Organization for Standardization (ISO) has advanced the revision of ISO 19011 to the Final Draft International Standard (FDIS) stage.
The International Medical Device Regulators Forum (IMDRF) has published a playbook to help regulators use shared approaches when reviewing medical devices, known as regulatory reliance.
The German Institute for Standardization (DIN) has published DIN SPEC 92006, introducing the first unified framework for artificial intelligence (AI) testing tools and setting clear requirements for how these tools should be designed and used.
The Organisation for Economic Co-operation and Development (OECD) has released a report examining how governments can improve regulation by making better use of standards, measurement, and assurance systems, known as quality infrastructure (QI).
The revision of ISO 9000, the international standard that defines the basic concepts and vocabulary of quality management, has reached the Final Draft International Standard (FDIS) stage, the final step before publication.
A new international standards committee has been created to develop standards for digital product passports (DPPs), systems designed to share key product information across the entire lifecycle and improve transparency and circular economy practices.
Global Accreditation Cooperation Incorporated has launched its new official website, providing a central online platform for the organization that became the single global body for international accreditation cooperation.