GMP-certified testing suites strictly qualifying active pharmaceutical ingredients (APIs) and critical excipients for paramount global regulatory compliance.
BrownBiology Laboratory operates specialized GMP-certified frameworks testing absolute compliance for all raw materials integrated into the pharmaceutical supply chain.
Both raw APIs and formulated excipients emphatically require deep safety assessments verifying they are fully fit to initiate downstream pharmaceutical preparation, matching all Ph.Eur. and USP mandates.
Our dedicated hubs draw from over two decades of raw matrix handling, powered by widening suites of sophisticated analytic technology and heavily trained lab directors.
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Equipped with deep-state technologies isolating raw material parameters from heavy trace elements to polymorphism profiling.
UV, DAD, FLD, RID, CAD, CD, EC, ELSD and MS
FID and MS for residual solvents and volatile impurities
Coulometric and volumetric moisture determination
IR (with ATR) and UV-VIS spectrophotometry
For extreme precision in heavy metal trace detection
High-throughput acid-base and red-ox reactions
Polymorphism and melting point determination
Determine profile of material particle size via laser diffraction
Conductivity, Index of refraction (Refractometer), Polarization (Polarimeter)
Vacuum ovens for curing/aging and Muffles for high-temp procedures
GMP-certified modules running globally compliant protocols strictly adhering to both USP and Ph.Eur. framework architecture natively.
Functioning as the premier gateway checkpoint for colossal pharmaceutical networks moving sensitive materials across continents.
Fitted with multi-layer separation tech, hypersensitive atomic mapping, and automated titration lines driven by veteran engineers.