API Standards

Manasa Life Sciences is dedicated to providing high-quality Active Pharmaceutical Ingredients (APIs) that comply with international pharmacopeial standards (USP, EP, JP) and regulatory guidelines (FDA, EMA, WHO).

Our APIs undergo rigorous testing for identity, purity, potency, and stability using validated methods such as HPLC, GC, NMR, FT-IR, KF, TGA, and Mass Spectroscopy. We support both qualitative and quantitative analysis, personalized to client-specific applications. Each batch is delivered with complete regulatory documentation, including Certificates of Analysis (CoA), Material Safety Data Sheets (MSDS), and Analytical Testing Reports(ATR), ensuring full traceability and regulatory compliance.

We maintain strict storage conditions for temperature-sensitive materials, using sealed, labeled containers to preserve stability and product integrity. Shipments are handled under ambient, refrigerated, or frozen conditions as required. We use validated insulated packaging and real-time temperature monitoring to ensure product integrity during global transit. All reference standards are packaged in tamper-evident (Amber vials, transparent vials) chemically inert containers, clearly labeled with all critical information. Customized labeling is available to meet regulatory or customer-specific needs. Materials with retest dates are periodically re-evaluated using validated methods. Products are not released beyond their retest or expiry date without verification and an updated CoA.

We are committed to delivering high-purity, well-characterized reference standards supported by scientific accuracy, proper documentation, and reliable global logistics. Our end-to-end quality system ensures that our API reference standards arrive ready for use, with confidence in stability, traceability, and compliance.