Kiwa Stories - Articles

In Celebration of International Women’s Day, we recently interviewed six of our female employees to find out how they are experiencing gender equality and inclusion in their careers and at Kiwa.

We Care is a management standard for the implementation and certification of sustainability requirements at company sites and in supply chain management for companies in the food industry. From cultivation in the countries of origin to the domestic supermarket, We Care certified companies act with their partners for a fair and environmentally friendly production of food. Learn more in our latest article.

When it comes to food safety, there’s an excess of certification programs out there to choose from to ensure the safety and quality of a food or beverage product. The infinite number of options can make it challenging for producers to decipher which certification is right for them. This is where ASI Food Safety (member of Kiwa Group) comes in. ASI is here to simplify the complex landscape of certification.

Colorless, odorless, tasteless: hydrogen is a seemingly humble element, yet we can’t stop raving about it. Green hydrogen is a key player in the generation of sustainable and cleaner energy,  addressing the urgent problems of carbon emissions, climate change, and energy security. Read more in our latest article.

The necessity for cybersecurity measures in the food industry is rapidly evolving, highlighting the critical demand for enhanced security measures to preserve food safety. In fact, the industry faces serious challenges due to the increasing digitization of food processes and reliance on interconnected technologies. Read more in our latest article.

At Kiwa, we offer comprehensive services tailored to Autonomous Driving (AD) testing, empowering the future of public transport. Learn how ZF transport systems and our partnership are revolutionizing public transport in Rotterdam, setting new industry standards for trust, efficiency, and sustainability.

The HVAC (Heating, Ventilation, Air Conditioning) industry — together with kitchen appliances — is an industry that is rapidly changing and developing. Like other industries, HVAC is no stranger to today’s cyber security challenges. The risks are multifaceted, from unsecured IoT (Internet of Things) devices in homes to potential threats to HVAC companies' production sites. Read more in our latest article.

The Portuguese wine sector continues to experience great growth and interest. In fact, wine tourism is thriving in the country, drawing domestic and international visitors to picturesque vineyards. As a qualified Certification Body for sustainable wines, Kiwa Portugal is pleased to announce our very first certification with the PSVA — the Sociedade Agrícola da Encosta do Guadiana, Lda wine farm.

In the dynamic realm of medical device development, the journey from conceptualization to market availability is intricate and demands meticulous evaluation at various stages. This text explains the processes of pre-clinical and clinical evaluations, essential components in ensuring the safety, performance, and regulatory compliance of medical devices. 

The persistent digital threat in the Netherlands — and beyond — continues to soar and evolve. Nation-states employ cyberattacks to further their geopolitical aims, and cybercrime, serving as a lucrative business model, inflicts harm on individuals and entities. Organizations must become more digitally sound due to increasing cyber threats, making compliance with legislation and certification more critical than ever.

Vinçotte, member of the Kiwa group, was recently contracted by Belgoprocess for visual inspection and thickness measurements of bunkered storage tanks at their wastewater treatment plant. Vinçotte's robotics partner hibot supplied the Floatarm, an articulated arm robot for multifunctional NDT inspections as a solution.

The Medical Devices Regulation (MDR 2017/745/EU) is a significant step forward in aligning European Union legislation with technological advancements, advancements in medical science, and the evolution of legal frameworks. By understanding the MDR requirements, manufacturers can navigate the intricate landscape of compliance and contribute to safer and more effective medical devices in the European market. 

Many wind farms have now been in operation for a while and are starting to notice wear and ageing. For plant managers, this means an increased challenge to ensure that the wind farms continue to produce renewable energy efficiently. This means that maintenance, inspections and upgrades are becoming increasingly important.

As AI technology takes flight, there's a growing urgency to investigate its influence on medical devices. In this article we will explore the complex world of AI-based medical devices, emphasizing the need for rigorous clinical evaluations and robust regulatory compliance. 

PPI Quality & Engineering, a Kiwa company headquartered in Houston, Texas, provides professional engineering, quality assurance, and auditing services to the energy industry clients around the world. Read all about PPI’s evolution of energy services, and their services for the global supply chain in our latest article.

By adhering to ISO 13485, organizations can establish a comprehensive quality management system that not only ensures regulatory compliance but also enhances overall performance and safety. Let's explore the manifold benefits this standard brings to your organization in the context of the medical device industry.