Explore Kiwa's expertise and comprehensive range of services and solutions across industries and beyond.
Consumers require quality, safety and traceability of Food, Feed and Agriculture products sourced from suppliers who produce in a fair, responsible and environmentally friendly way. Kiwa offers global certification, verification and (production and equipment) control services to help you as a retailer, supplier, producer, logistics partner or farmer, to build customer confidence.
Cyberattacks and threats can cause grave disruptions. Sensitive data can be lost or stolen and industrial processes could be halted, ultimately causing stagnation of production with revenue loss. It could even cause customers and public to lose trust in a company which became a victim of a cyberattack, leading to reputation damage.
Kiwa contributes to sustainable solutions for our today’s and future energy supply. We offer a one stop shop service to cover safety and quality demands for energy installations and related components. Together with the manufacturing industry, governments, network operators, education centers and other parties, we set the standard in acceptable technologies and solutions. We fulfil an extended portfolio in the entire market chain with a unique mix of years of knowledge, in house experience, innovative power and geographical presence. Kiwa can support you by delivering extended services in testing and certification of products and systems, verifications and consultancy and training. Our experts can help you in many different areas, such as renewable gas, hydrogen, electrification, internet connectivity, energy storage systems and carbon footprint. As a partner for progress we want both you and the world to take a step forward.
We help you with services that ensure smooth operations and optimal manufacturing output from your production processes ensuring unplanned downtime is minimized. We do this through testing and inspection of the production equipment you use for your manufacturing process. This to ensure, availability, safety, quality and compliance with applicable standards.
Medical devices manufactured or traded in the EU must comply with EU legislation in safety and health. This means they must be conformed to the pertaining product directives and regulations and must be CE marked.
Evidence of the quality, safety, healthiness and durability of the products, from concept to consumer.
We understand the importance of sustainability in today's world. It is no longer just an option, but a necessity for the well-being of our planet and future generations. That's why we are here to support you as your dedicated partner in driving positive change.
Is a certificate still valid? Search our certification database for certifications issued by Kiwa and check their validity.
At Kiwa, we are committed to contributing to a safer, more sustainable, and more secure world. Through our expertise in testing, inspection, and certification, we support businesses, governments, and society in addressing key challenges.
Discover the focus of Safety Week 2026, running from 5 to 9 October. This year, we introduce the Energy Wheel as a practical prompt to help colleagues recognize energy sources before work starts, especially during the Last-Minute Risk Assessment.
EEW Energy fromWaste Delfzijl B.V. recovers energy and raw materials from waste streams and was recently certified by Kiwa at Level 1 of the CO2 Performance Ladder version 4.0. This means that EEW has demonstrated that its CO2 management system meets the strengthened requirements of the updated Handbook 4.0 of the CO2 Performance Ladder. With this certification, EEW underlines its ambition to structurally monitor, achieve and safeguard its sustainability goals.
Hydrogen storage systems must perform safely and reliably under demanding operating conditions. Comprehensive testing plays a key role in verifying their durability, performance and compliance before they enter the market. To meet this demand, Kiwa ET has expanded its hydrogen testing infrastructure and can now perform standardized testing on hydrogen pressure tanks with volumes of up to 600 litres.
Medical device manufacturers operate in an increasingly complex regulatory environment. While compliance requirements such as the Medical Device Regulation (MDR) apply across the industry, the path to certification is rarely the same for every organization.
