API Standards

Manasa Life Sciences is committed to providing high-quality Active Pharmaceutical Ingredients (APIs), as well as well-characterized Primary and Working Standards. All our products meet international pharmacopeial standards such as USP, EP and follow global regulatory guidelines from agencies like the FDA, EMA, and WHO.

Our API Standards are thoroughly tested for identity, purity, potency, and stability using validated methods such as HPLC, GC, NMR, FT-IR, Karl Fischer (KF), TGA, and Mass Spectrometry. We offer both qualitative and quantitative testing, customized to meet the needs of our clients. Each API Standard comes with complete documentation, including a Certificate of Analysis (CoA), Material Safety Data Sheet (MSDS), and Analytical Testing Report (ATR), ensuring full traceability and compliance.

To protect temperature-sensitive materials, we store them in sealed, clearly labeled, chemically safe containers under controlled conditions. Shipments are made under ambient, refrigerated, or frozen conditions as needed, using validated packaging and real-time temperature monitoring to maintain product quality during international shipping. All reference standards are packed in tamper-evident amber or transparent vials, with clear labels showing all key information. We also offer custom labeling to meet specific client or regulatory needs. Products with retest dates are regularly re-evaluated, and nothing is shipped past its retest or expiry date without proper testing and an updated CoA.

We are dedicated to delivering high-purity APIs and Primary and Working Standards supported by accurate science, complete documentation, and dependable global logistics. Our quality system ensures that all our products are stable, traceable, and compliant ready for immediate use.