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 Farm 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.
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.
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.
