Kiwa Stories - Articles

At our recent RAPS session in Lisbon, one message clearly emerged: under MDR (EU) 2017/745, clinical evidence is a continuous lifecycle process that depends on the strength of the entire ecosystem.

Discover how Vestas Offshore Wind Belgium implemented Vinçotte - a Kiwa company’s Digi-Tags solution to optimize and simplify the statutory inspection process across its wind farm operations.

Discover how internationally recognized management system standards helped support quality, security, sustainability and continuous improvement in the Digital Realty client case.

Know more about a joint development project between Kiwa Sweden and a wind power industry operator. The aim was to develop and validate methods for assessing the potential life extension of wind turbine towers and foundations across several wind farms, with a focus on data-driven analyses and more efficient approaches for future lifetime assessments.

HortaPronta is a Portuguese horticultural producer that has maintained a close partnership with Kiwa for over 20 years, following a shared journey focused on food safety certification, continuous process improvement and compliance with the requirements of both national and international markets.

In recent years, the battery industry has been moving through a period of rapid transformation. Increasing demand for electric vehicles, energy storage and light transport has not only driven innovation, but also pushed sustainability, transparency and responsible sourcing to the forefront of regulatory expectations. Against this backdrop, the European Union introduced the Battery Regulation (EU 2023/1542): a comprehensive framework designed to ensure that every battery placed on the EU market contributes to a more transparent and circular economy.

The global race towards carbon neutrality is accelerating the deployment of offshore renewable energy. Among the most promising technologies, floating offshore wind stands out as the key to unlocking deep‑water wind resources and enabling large‑scale clean energy production. Portugal is playing a pivotal role in this transition — with Kiwa Portugal recognised as a leading technical partner in this emerging market.

Biological evaluation is a fundamental element in demonstrating the safety of medical devices and compliance with Regulation (EU) 2017/745 (MDR). The ISO 10993 series represents the internationally recognized standard for assessing the biocompatibility of materials and devices throughout their entire lifecycle.

At Kiwa Medical, the four eyes principle is more than a procedural requirement—it is a daily safeguard for technical quality and regulatory confidence. Whether applied to peer reviews of audit reports, technical documentation assessments, or certification decisions, involving a second qualified reviewer before finalization adds real and measurable value.

Volume calibration of storage tanks is a vital part of safe process‑industry operations and ensures the reliability of trading liquid products sold by volume. Accurate volume data is essential for the storage, handling and sale of chemicals, fuels and other industrial liquids, as well as for process control and fulfilling regulatory requirements.

This is an important step in Kiwa’s continued development of services for the medical device sector. Applicant status means Kiwa has entered the formal process toward recognition as an MDSAP Auditing Organization.

Annex XVI of EU MDR 2017/745 covers specific product groups that do not have a medical intended purpose, yet are used on the human body and inherently carry certain risks. Although these products are not intended for diagnosis or treatment, they are included within the MDR framework due to their potential impact on human health and safety.

From 5 to 8 May 2026, Lisbon will host a new edition of RAPS Europe, one of the leading European events dedicated to Regulatory Affairs in the life sciences and medical devices sector.

On 16 March 2026, the European Commission hosted the High-Level Conference on Medical Devices: Innovation and Patient Safety in Brussels, an event that brought together key institutional representatives, regulatory authorities, industry experts, and stakeholders from across Europe.

We are proud to announce that Kiwa Nederland has extended their CBTL accreditation with electrical safety testing of medical devices. This milestone allows us to support medical device manufacturers even more effectively in demonstrating compliance with international standards, not only for EMC, but now also for electrical safety. 

As a testing, inspection, and certification company, our sustainability sector is all about harnessing ‘Our Power’ to make a difference. Our work helps businesses around the world adapt to shifting regulations, measure their environmental performance, and build the transparent practices that stakeholders increasingly demand and that our planet needs.  In this article, Justin shares more about Kiwa's sustainability solutions and what they mean for businesses working toward a greener future.