We provide comprehensive Raw Material and Excipient Analysis to ensure compliance with pharmacopoeial standards and regulatory expectations.

Our services include the identification, purity, potency, and safety evaluation of raw materials and excipients, following relevant monographs from USP, EP, BP, IP, JP, and other global pharmacopeias. Each analysis is conducted using validated methods and advanced instrumentation under GMP-compliant conditions.

With a strong focus on quality, traceability, and regulatory readiness, our analytical testing supports:

• Incoming material qualification
• Supplier verification and audits
• Regulatory submissions and batch release

Partner with us to ensure your materials meet the highest standards of quality, consistency, and compliance.