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Explore our press releases and news updates. Delve into detailed press kits for information on our work. If it’s UL and newsworthy, it’s here.
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We help people achieve what’s possible by empowering trust. Businesses, industries, governments, regulatory authorities and the public put their trust in us so they can make smarter decisions.
Explore our business intelligence-building digital tools and databases, search for help, review our business information, or share your concerns and questions.
A secure, online source for increased visibility into your UL project files, product information, documents, samples and services.
Verify the certification of products and components with Product iQ. Advanced search and filtering make it easy to access guide information, alternative products and more.
Drive positive change with our offerings that expertly address your business needs or industry challenges.
Our technical, regulatory and clinical expertise substantiates trust in medical technology, healthcare delivery networks and consumer wellness devices. We’ll help you manage regulatory challenges and bring safer products to market faster.
For medical devices with direct or indirect patient contact, the biological safety of the device and its intended use should be considered. We can perform biocompatibility evaluation studies in accordance with ISO 10993-1:2009.
UL tests respiratory and ventilation devices to the ISO 18562 series of standards to help manufacturers provide the necessary data to bring products to the marketplace.
Safer products are paramount to long-term business success, a strong brand and happy, loyal consumers. Protect your brand, differentiate your products, mitigate risk, and demonstrate your commitment to consumer safety and health.
Our custom testing services are aimed at helping you create safe and user-friendly devices while achieving required regulatory compliance.
Our Data Acceptance Program (DAP) provides a means for UL to accept externally generated test data in support of UL Mark certification. While we maintain extensive test facilities, customers can utilize their own or third-party facilities for product testing via this program.
We offer a full suite of services aimed at helping you communicate compliance to the applicable standards and the suitability of their devices for security and use in electrical labs, scientific research labs and factory automation.
Our EMC testing facilities provide cost-effective assessments of electronic products with custom testing solutions that enhance process efficiency and reduce testing cycles, helping you meet demanding time-to-market needs.
We’ll help you understand and comply with federal and state regulatory requirements for EPCS applications.
In today’s competitive marketplace, trust, safety and quality are prime differentiators. Tap into the UL Mark Certification service to make safety a priority, help you gain market access, and add real value to your brand.
The Green Laboratory Practices Certification from UL Environment helps hospitals and other medical laboratory facilities communicate their comprehensive efforts toward reduced environmental impact of operations.
UL offers a variety of hazardous location training courses that use both practical and theoretical assessments to elevate a candidate’s core competencies related to standard safety regulations.
As an INMETRO accredited test agency for medical equipment, we can provide the mandatory product certification and factory inspections required by the regulations. The UL-BR Mark can help simplify your access to the Brazilian market.
The regulatory approval process is often complex and ill-defined. UL provides manufacturers with testing and compliance assistance to help ensure faster clearance of FDA 510(k) submissions related to respiratory and ventilation devices and accessories.
Our objective verification of your marketing claims helps you stand out in a crowded marketplace. Independent substantiation of your marketing and advertising claims builds trust with your customers, empowering them to choose your product with confidence.
For medical devices with direct or indirect patient contact, the biological safety of the device and its intended use is critical. UL can perform biocompatibility evaluation studies in accordance with ISO 10993-1:2009.
The UL CAP Evaluation reviews documentation related to processes concerning medical devices and network connected device cybersecurity. The UL CAP Certification process evaluates documents and process assessment and also conducts software testing.
We have developed sharable databases, open-source tools and applications that will enable a broader community of researchers and manufacturers to implement secure medical device interoperability.
Our package testing services help ensure safe and sterile delivery of critical medical devices.
Our usability suite of testing services are aimed at helping you create safe and user-friendly devices while achieving required regulatory compliance.
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