API Standards

Our API standards are severely tested for identity, purity, potency, and stability using validated analytical techniques such as HPLC, GC, NMR, FT-IR, Karl Fischer (KF), TGA, and Mass Spectrometry. We offer both qualitative and quantitative testing, customized to meet specific client requirements. Each API standard is supplied with comprehensive documentation, including a Certificate of Analysis (CoA), Material Safety Data Sheet (MSDS), and Analytical Testing Report (ATR), ensuring full traceability and regulatory compliance.

To protect temperature-sensitive materials, products are stored in sealed, clearly labeled, chemically compatible containers under controlled conditions. Shipments are carried out under ambient, refrigerated, or frozen conditions, as required, using validated packaging and real-time temperature monitoring to maintain product integrity during international transportation. All reference standards are packed in tamper-evident amber or transparent vials, with clear labeling that includes complete product information. Custom labeling is also available to meet specific client or regulatory needs.

Products assigned a retest date are periodically re-evaluated using validated methods, and no material is supplied beyond its retest or expiry date without proper verification and an updated CoA.

We supply APIs and reference standards to markets across Asia, Europe, Africa, the GCC, and the UAE, ensuring reliable delivery, complete traceability, and adherence to Good Documentation Practices for APIs and finished dosage forms. With a strong commitment to quality, accuracy, and dependable global logistics, Manasa Life Sciences delivers stable, compliant, and ready-to-use pharmaceutical materials for research, development, and commercial applications.