About Us
MARYA designs, builds and qualifies integrated aseptic fill-finish lines for vials, pre-filled syringes (PFS), cartridges, ampoules and RTU, complete with isolator containment to OEB 5, formulation, pure utilities and cleanroom, engineered to EU GMP Annex 1 and FDA aseptic expectations. Founded in 2014 and built on 20+ years of team expertise, MARYA operates a 10,000 m2 integrated manufacturing facility, exports to 70+ countries and serves 300+ pharmaceutical manufacturers worldwide. Six engineering disciplines are integrated into every line under one accountable team: aseptic filling, isolator/RABS containment, formulation skids, PW/WFI/steam utilities, cleanroom build and end-of-line processing, so sterility, containment, data integrity and qualification are resolved before they reach your qualification team. Every line is delivered with DQ/IQ/OQ/PQ and FAT/SAT qualification, ISO 9001 and CE certified quality, and 24/7 global lifecycle support.
