Time to market is a critical factor in monetizing business opportunities, and its importance is growing. UL's trusted compliance expertise aids our customers in cutting through regulatory complexities, helping to create a competitive advantage.
With comprehensive knowledge of the regulatory requirements impacting consumer product performance, construction and composition, UL’s team of quality assurance experts help develop testing programs for a wide range of regulations including the European Union regulation on chemicals and their safe use (REACH); Consumer Product Safety Improvement Act (CPSIA); Restriction of Hazardous Substances (RoHS) Directive; and China’s mandatory textiles and apparels standard (GB 18401). UL’s global regulatory testing capabilities help ensure compliance for every country in which our customers source or sell.
UL is accredited by:
Additionally, UL is registered with the Consumer Product Safety Commission (CPSC) as an accredited laboratory for CPSIA third-party testing.
UL’s active involvement in the development and revision of international product safety standards and unmatched industry expertise help us identify hazards early in the production cycle to reduce product development cost and increase speed to market. Our leadership in the compliance space helps ensure that our customers meet current regulatory demands and are aware of emerging regulations.
|American Society for Testing and Materials (ASTM) Internationa||Voluntary consensus standards used to improve product quality, enhance safety, and facilitate market access and trade|
|American Spice Trade Association (ASTA)||Industry standards for analytical testing of spices|
|Association of Analytical Chemists (AOAC)||Standardized chemical analysis methods designed to increase confidence in results of chemical and microbiologic analyses|
|British Pharmacopoeia Convention||Authoritative official standards for pharmaceutical substances and medicinal products in the UK|
|British Standards Institution (BS)||Multinational business services provider; principal activity is the production of standards and the supply of standards-related services|
|California Proposition 65||Requires the State of California to publish a list of chemicals known to cause cancer or birth defects or other reproductive harm; requires businesses to notify Californians about significant amounts of chemicals in the products they purchase, in their homes or workplaces or that are released into the environment|
|Canadian Chemicals Management Plan||The Chemicals Management Plan protects human health and the environment by assessing chemicals used in Canada and by taking action on chemicals found to be harmful|
|China GB||Chinese national standards, which are issued by the Standardization Administration of China (SAC), the Chinese National Committee of the ISO and the IEC|
|China New Chemical Legislation||This regulation is similar to REACH in the EU and is also known as “China REACH”|
|Consumer Product Safety Improvement Act (CPSIA) of 2008||Authorized a variety of new regulations and testing requirements for children’s products and some non-children’s products|
|EU Registration, Evaluation, Authorisation and Restriction of Chemical (REACH) Substances||Addresses the production and use of chemical substances and their potential impacts on both human health and the environment by streamlining and improving the former legislative framework on chemicals of the European Union (EU)|
|EU Toy Safety Directive 2009/48/EC||Foundation of toy safety legislation and enforcement in the European market|
|Food Chemical Codex (FCC)||Compendium of internationally recognized standards for determining the purity and quality of food ingredients|
|German Institute for Standardization (DIN)||The acknowledged national standards body representing German interests in European and international standards organizations|
|International Featured Standards (IFS)||Evaluation system for all companies supplying branded food products to retailers; applicable to production, processing of the product and packaging into smaller units; provides uniform formulations, uniform audit procedures and mutual acceptance of audits|
|Japan Pharmacopoeia Convention||Defines the standards for specifications and the methods of testing to ensure overall quality of all drugs in principle; plays a role in clarifying the criteria for quality assurance of drugs that are recognized to be essential for public health and medical treatment in Japan|
|Standards associated with the Korea Certification (KC) Mark||Korea Certification (KC) Mark is required to sell certain products in Korea, including electrical/electronic equipment and textile products|
|Restriction of Hazardous Substances (RoHS) Directive||Directive restricts the use of six hazardous materials in the manufacture of various types of electronic and electrical equipment|
|U.S. Pharmacopeial Convention||Standards for the identity, strength, quality and purity of medicines, food ingredients and dietary supplements manufactured, distributed and consumed worldwide; enforceable in the United States by the Food and Drug Administration and developed and relied upon in more than 140 countries|
|U.S. Toxic Substances Control Act (TSCA)||Prohibits the manufacture or importation of chemicals that are not on the TSCA Inventory (or subject to one of many exemptions)|