Fairfield, New Jersey

Our Facility

Advanced laboratories and manufacturing capabilities meeting the highest industry standards.

Advanced Manufacturing Complex

Our Fairfield, New Jersey headquarters houses a comprehensive ingredient technology facility designed to meet the most demanding requirements for pharma-grade production standards.

With over 10,000+ square feet of laboratory and production space, we maintain separate areas for R&D, pilot-scale production, and kilo-scale manufacturing.

Our production facilities are equipped to seamlessly scale from lab to kilo-scale manufacturing with glass and stainless-steel reactors ranging from 50 to 100 liters, alongside large-scale rotary evaporators, advanced filtration units, and dedicated prep-chromatography systems.

Laboratory equipment and facilities

Facility Highlights

10,000+ sq ft manufacturing space
Dedicated R&D laboratories with fume hoods
Pilot-scale and kilo-scale production suites
Glass & stainless-steel reactors (50-100L)
Temperature control (-90°C to +200°C)
Advanced analytical laboratory
Comprehensive quality control systems
Secure chain-of-custody protocols
Large-scale rotary evaporators
Prep-chromatography systems

Manufacturing Capabilities

Advanced equipment and infrastructure designed for pharmaceutical-grade production from milligrams to kilograms.

Synthetic Laboratories

Fully equipped fume hoods, dedicated bench space, and advanced purification systems for complex syntheses.

Temperature Control

Cryogenic capabilities (-90°C) to high-temperature reactions (200°C+) with precise control.

Production Suites

Segregated production areas with dedicated equipment to prevent cross-contamination.

Analytical Laboratory

2 HPLC-MS units, Prep-HPLC, UHPLC, GC-MS, NMR, FTIR, UV-Vis, polarimeter, and titration modules.

Quality Control

Dedicated QC lab with validated methods and equipment for release testing.

Documentation Systems

Electronic batch records, chain of custody, and comprehensive quality documentation.

Analytical Instrumentation

Comprehensive analytical capabilities for complete characterization and quality control of bioactive compounds.

Chromatography

  • 2 HPLC-MS systems with UV and PDA detection
  • UHPLC for rapid method development
  • Prep-HPLC for large-scale purification
  • Chiral HPLC for enantiomeric analysis
  • GC-MS for volatile compound analysis
  • Custom method development & validation

Spectroscopy & Analysis

  • NMR (¹H, ¹³C, 2D experiments)
  • High-resolution mass spectrometry
  • FTIR spectroscopy
  • UV-Vis spectrophotometry
  • Polarimeter for optical rotation
  • Mettler Toledo titration modules

Physical Testing

  • Melting point determination
  • Optical rotation (polarimetry)
  • pH and conductivity measurement
  • Moisture content (Karl Fischer)
  • Organoleptic evaluation
  • Precision microbalances

Inside Our Facility

Take a look at our advanced laboratories, specialized equipment, and quality-controlled production environments.

Production Laboratory

Production Laboratory

Manufacturing operations

Precision Analysis

Precision Analysis

Analytical chemistry

Process Development

Process Development

Pilot-scale production

Production Reactors

Production Reactors

Kilo-scale synthesis

Pressure Reactor

Pressure Reactor

Specialized synthesis

R&D Laboratory

R&D Laboratory

Research & development

HPLC-MS System

HPLC-MS System

Analytical testing

Manufacturing Evaporator

Manufacturing Evaporator

Large-scale purification

R&D Evaporators

R&D Evaporators

Process development

Laboratory Workspace

Laboratory Workspace

Advanced equipment

HPLC System

HPLC System

Quality control

Facility Lobby

Facility Lobby

Welcome entrance

Quality Assurance & Compliance

Rigorous quality systems ensuring consistency, safety, and regulatory compliance for every production run.

Quality Control Systems

Rigorous quality control protocols with comprehensive analytical testing, validated processes, batch documentation, and certificate of analysis for every production run.

Pharma-Grade Standards

Manufacturing practices following pharma-grade standards under the spirit of GMP with controlled environments, validated equipment, and comprehensive documentation systems.

Quality Management

Comprehensive quality management system with documented procedures, change control, CAPA, and ongoing training programs for all technical staff.

Environmental Health & Safety

Comprehensive EHS program including chemical hygiene, waste management, emergency response, and employee safety training.