USP 42-NF 37 United States Pharmacopoeia and National Formulary Testing Standard

EUROLAB laboratory provides testing and compliance services within the scope of USP 42-NF 37 standard. The United States Pharmacopoeia and National Formulary (USP-NF) contains standards for drugs, dosage forms, drug substances, excipients, biologics, compound preparations, medical devices, dietary supplements, and other therapeutics.

The current version, officially recognized by the USP, is applicable by the US Food and Drug Administration for drugs manufactured and marketed in the United States. USP standards are used in more than 140 countries around the world.

More than 4.900 monographs with specifications for identity, potency, quality, purity, packaging, and labeling for substances and dosage forms, over 350 general chapters, focus-specific charts, and composite charts that provide clear, step-by-step guidance for assays, tests, and procedures. The index helps you find the information you need.

Quality control is essential for quality assurance, regulatory affairs, research and development, method development services and corporate governance.

USP–NF monographs and methods can help:

• Ensuring compliance with required US quality standards;
• Working according to world-recognized standards of precision and accuracy;
• Validating test results against proven benchmarks;
• Establishing and validating internal standard operating procedures.

EUROLAB assists manufacturers with USP 42-NF 37 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.