Latest news from Kiwa

Kiwa at HOST

Kiwa will be present at HOST 2025, the international trade fair dedicated to the world of food service and hospitality, which will be held in Milan from October 17 to 21, 2025. We look forward to seeing you at Hall 3P – Stand G60 to discover all our solutions for the Ho.Re.Ca. and Food sectors.

Host Milano 2025 logo, International Hospitality Exhibition, October 17-21, 2025, Fiera Milano

CPR 2024 - reshaping the future of construction

One of the most significant changes introduced by CPR 2024 is the integration of technical and environmental performance into a single, consistent and verified framework for construction products.

Kiwa at Hydrogen Technology Expo Europe

Kiwa is pleased to announce its participation in the Hydrogen Technology Expo Europe, taking place from 21 to 23 October 2025 at Hamburg Messe, Germany.

New Regulation Brings Clarity and a Transition Period for Drinking Water Directive in Italy

From July 2025, Italy will enforce new regulations under Legislative Decree 102/2025, aligning with the EU Drinking Water Directive. Learn how Kiwa can support your compliance during the transition period.

Live webinar series: Your step-by-step guide to carbon verification

Titled "Journey to Carbon Verification", the series will explore the ISO 14064 standards and provide insights into the key steps involved in carbon reporting, management, and third-party verification. The sessions are designed for sustainability professionals, compliance officers, and anyone responsible for carbon and ESG reporting within their organization.

Overview of AI-Enabled SaMD and SiMD Devices

Artificial Intelligence (AI)-based software medical devices are revolutionizing the healthcare sector in diagnosis, treatment, and patient management. AI-powered Software as a Medical Device (SaMD) and Software in a Medical Device (SiMD) applications cover a wide range of solutions, from medical decision support systems to patient monitoring tools.

Medical equipment close-up in a healthcare facility, displaying vital signs on a monitor, with healthcare professionals in scrubs and masks in the background

Placing medical devices in Great Britain and Northern Ireland: key differences and timelines

The rules for placing medical devices on the Great Britain (GB) and Northern Ireland (NI) markets differ primarily in terms of the timelines and regulatory frameworks

Kiwa at PRSE 2025

The plastics industry is transforming, with recycling and sustainability at the heart of its future. As regulations become stricter and consumers demand more environmentally friendly solutions, ensuring quality, compliance, and innovation in recycled plastics is more important than ever.

Fit4DW materials database speeds up certification

Kiwa, DVGW CERT, and figawa are launching the Fit4DW materials database at ISH 2025. This platform simplifies the certification of drinking water materials, ensuring compliance with EU regulations. By centralizing verified data, it reduces certification time by up to nine months, saving costs while ensuring safe, high-quality water.

Medical device registration in Great Britain and Northern Ireland

Registration of certain medical devices which are reusable Class I devices, upclassified Class I devices, and/or reliant on expired/expiring CE certificates in Great Britain (GB) and Northern Ireland (NI).

Kiwa and Vinçotte: Key Partners in the Horizon Europe SYRIUS Project

Kiwa and Vinçotte are proud to be key partners in the Horizon Europe SYRIUS project, which aims to revolutionize steelmaking by integrating hydrogen into the production process. This groundbreaking initiative will significantly reduce CO2 emissions and improve energy efficiency. With Kiwa's expertise in safety and certification, and Vinçotte’s focus on compliance, the project sets new standards for sustainable steel production and industrial innovation.

What are the requirements for registering medical devices with MHRA?

To register medical devices with the MHRA, manufacturers must follow specific requirements and procedures.  In this article you will find the key steps and requirements.

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