Facility Footprint
- Research facility – 3,500 sft.
- Pilot plant – 3,000 sft.
- Non-GMP manufacturing facilities – 90,000 sft. (site 2)
- GMP manufacturing plant – 37,800 sft.
Encompassing fine chemicals, reagents, key starting materials, regulatory starting materials and API.
Catering to Pharmaceuticals, Agrochemicals, cosmeceuticals, electronics, nutrition and other performance chemicals.
Manufacturing
Validated Analytical Methods
Redox Scientific delivers comprehensive analytical method validation, advanced impurity profiling, and robust stability testing to ensure total drug substance and product integrity. Equipped with state-of-the-art capabilities-including ICP-MS, LC-MS/MS, HPLC, UPLC, GC, GC-HS, GC-MS, IR, KF, and auto-titrators-we specialize in solving complex analytical challenges from IND-enabling studies and clinical trials through commercialization. Our expert team ensures strict regulatory compliance for genotoxic impurities, trace metals, and photostability. Partner with us for precise quality control, reliable reporting, and custom method development that accelerates your path to market.
US-Based Leadership, Global Scientific Excellence
Documented Regulatory Readiness
Facility At Glance
- Dedicated reactors for small scale cGMP production.
- No down time – brand new facility.
- Pressure reactions up-to 425 PSI / 30 Kg/cm2.
- Hassel free regulatory cGMP documentation.
- Low endotoxin and low trace metals for parental applications.
- Reduce Particle Size with Milling to improve bioavailability and proper delivery.
- 5 Class D cGMP Suites with 16 AHUs to manufacture 5 products simultaneously.
- QC: Class C Micro Suites, Waters Acquity UPLC, Agilent 7890 GC-MS/HS, Agilent LC-MS, Metrohm Auto titrator, Meteohm KF, Agilent UV, Agilent FTIR and ICP-MS.
Certified Excellence
Demonstrating our commitment to quality, regulatory compliance, and operational excellence through globally recognized certifications.
ISO 9001 CERTIFICATE
ISO 14001 CERTIFICATE
ISO 45001 CERTIFICATE
