REACH Registration: A Comprehensive Guide for Testing Laboratories and Businesses
REACH registration is a regulatory requirement for the EU chemical market and also a business opportunity for contract testing labs worldwide
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REACH registration is a regulatory requirement for the EU chemical market and also a business opportunity for contract testing labs worldwide
Discover the purpose, importance, and development of NATO STANAGs. Learn how these standardization agreements enhance interoperability among member nations and adapt to modern challenges."
In the third annual "Chain Reaction" report, the most popular US fast food chains are graded on their use of antibiotics in food, specifically meat, as well as their policies and meat sourcing practices. Historically, antibiotics have been given to animals that...
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Protecting the environment is a primary goal of CLP regulations
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Flammability testing is a critical part of ensuring that Halloween costumes are safe for children and adults alike
TCLP testing is an essential tool for assessing the potential hazards of waste and ensuring environmental safety.
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FDA compliance in veterinary medicine testing is not only a regulatory requirement but also a benchmark for quality and safety in animal health products. Ensuring the safety and efficacy of veterinary drugs, devices, and food additives is a top priority that...
By using advanced analytical methods such as HPLC, GC-MS, LC-MS, FTIR, and NMR, pharmaceutical companies can accurately identify and quantify controlled substances, verify product quality, and meet regulatory standards.
Discover how proper labeling protects consumers, meets regulatory standards, and promotes safe usage of hazardous art materials.
The Substance Abuse and Mental Health Services Administration (SAMHSA) is a part of the U.S. Department of Health and Human Services whose main goal is the advancement of behavioral health. SAMHSA aims to reduce substance abuse and mental illness in the U.S. The...
ISO 10993 medical device biocompatibility testing is performed to observe how compatible a device is with living tissue. To be considered biocompatible, a device needs to cause no local or systemic response. Biocompatibility is determined through a series of tests...
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