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It contains standards for medicines, dosage forms, drug substances, excipients, biologics, compounded preparations, medical devices, dietary supplements, and other therapeutics. Offers convenient, comprehensive information for all phases of producing quality prescription, nonprescription, and compounded medicines; excipients; biologics; medical devices; and dietary supplements. It is essential for quality control, quality assurance, regulatory/compendial affairs, research and development, method development/analytical services, and corporate management. USP–NF monographs and methods can help to: - Ensure compliance with required U.S. quality standards - Work to world-recognized standards of precision and accuracy - Validate test results against proven benchmarks - Establish and validate in-house standard operating procedures, and specifications - Expedite new product development and approvals