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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.
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Access UL certification data on products, components and systems, identify alternatives and view UL guide information with Product iQ.
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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.
Our regulatory and safety testing for healthcare devices can help prevent hackers and cybercriminals from potentially compromising private and confidential healthcare data and placing patients at risk.
To create brand trust, OTC products, dietary supplements and medical devices should be tested to verify safety, quality, performance and marketing claims to confirm that products perform as expected.
To provide safer patient care, medical device and operational equipment requires certification to accepted standards.
Management system audits and product certifications for healthcare and medical device manufacturers.
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.
We help protect your brand’s reputation in the Internet of Things (IoT) by offering you interoperability and connectivity testing services that confirm your products perform in accordance with your claims.
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 501(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.
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