Kiwa Stories - Articles

In a world where artificial intelligence is evolving at lightning speed, ML6, a Belgian AI consulting and services company, stands out as a pioneer. Patrick Coomans, Global Product Owner of Cyber Security at Vinçotte (a Kiwa company) sat down with ML6 experts Rob Vandenberghe and Louis Vanderdonckt to discuss how ML6 is evolving, the role it plays in the AI landscape, and why trust is an absolute prerequisite for long-term value creation.

Kiwa PI Berlin advises Sonnedix on quality control through an agreement that includes factory inspection and auditing services, production supervision, ESG analysis and traceability, in-factory testing and in-house laboratory testing.

This case study highlights the challenges, expertise, and detailed process involved in testing liquid hydrogen (LH₂) systems, based on the experience of Kiwa as an independent testing laboratory. To understand what this work entails, this case study takes you through the landscape in which LH₂ technology is developing, the capabilities of Kiwa, and the step-by-step testing process that customers rely on.

The EU Carbon Border Adjustment Mechanism (EU-CBAM) is a key instrument of the European Union aimed at preventing carbon leakage and ensuring fair competition between EU manufacturers and importers from third countries. By aligning the carbon costs of imported goods with those produced within the EU, the mechanism supports the EU’s climate objectives while encouraging cleaner production globally.

CPR-2024 is not just about what you provide, but why. The updated regulation goes beyond compliance, setting a clear path toward sustainable, circular, and transparent construction practices. Digital product passports, environmental data in the DOPC, and strengthened oversight will shape the industry.

Under Article 52 and Annexes IX through XI of the Medical Device Regulation (MDR), it is the legal manufacturer's responsibility to select the appropriate conformity assessment route. However, as a Notified Body, we often observe confusion regarding what these assessments entail and which route is best. The correct choice depends on the device classification and the level of control the manufacturer maintains over design and production.

At Kiwa Assurance, we recognize that innovation is a constant in the medical device industry. But change comes with responsibility—especially when it comes to maintaining compliance under the MDR and ISO 13485. That’s where our Notification of Change (NoC) process plays a vital role.

Kiwa’s livestreamed, cloud-based inspection solution brings together drones, real-time collaboration, AI-driven analysis, and centralized data to transform how industrial assets are inspected and managed—making inspections safer, faster, and more connected.

Discover how AI and advanced imaging are reshaping concrete inspections—making them safer, faster and more cost-effective.

The revised European CPR-2024 could impact your business sooner than expected. Discover the five crucial developments every construction product manufacturer should be aware of and prepare for.

In close collaboration with innovation partner SkyeBase, Kiwa is setting new standards in intelligent yard inspection services. Combining the use of drones, data and specialized AI technology with experience-based human insight, we can guarantee that even the largest industrial sites remain safe, efficient, and future-proof.

Discover how Equans Digital is transforming industrial operations by bridging IT and OT, enhancing safety, and building digital trust. Learn why cybersecurity is the next evolution of operational safety.

In a world where transparency and integrity are non-negotiable, Chain of Custody (CoC) certification is becoming a strategic asset for food businesses. Whether you're handling fresh produce or seafood, CoC standards like GLOBALG.A.P. and MSC help ensure that certified products remain authentic, traceable, and undiluted throughout the supply chain.

For seasoned professionals in food safety and quality, this isn’t just a supply chain. It’s a risk landscape. Every product represents a journey through raw materials, feed, farming, processing, packaging, logistics, and retail. And every step must be controlled, certified, and transparent.

At Kiwa Assurance, we recognize that innovation is a constant in the medical device industry. But change comes with responsibility—especially when it comes to maintaining compliance under the MDR and ISO 13485. That’s where our Notification of Change (NoC) process plays a vital role.

With the introduction of the revised Construction Products Regulation (CPR), a lot is changing for manufacturers of construction products. The updated CPR will take effect gradually, depending on the product group. But what exactly does this European legislation entail? What can you expect? And why is it smart to start preparing now?