A Premier CDMO. FDA Registration #1210580.
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Compliance, Quality, Cost-effective

Our cGMP facility will manufacture your products and release through our Quality Control Laboratory where we implement validated methods and USP Monograph testing. We offer up to date, qualified instrumentation and diverse testing capabilities at a competitive outsourcing cost.

Analytical

Spectroscopy

•FT-IR

•UV-Vis

•Refractive Index

Wet Chemistry

•Titrations

•pH

•Specific Gravity

•TOC

•Karl Fischer

Chromatography

•HPLC-UV, RID, CAD

•GLC-FID

Physical Testing

•Viscosity

•LOD

•ROI

Microbiological

AET

Automated Analysis

•Rapid Microbial Testing

•Automated microbial ID system

Water Testing

•RO Water

Services

Raw Material Testing

•USP / NF

Methodology

•Development

•Validation

•Verification

•Transfer

•Optimization

Stability Program

•In-house storage

•Full testing

LIMS

•Sample tracking

•Trending

•Documentation

•Validated and 21CFR11 compliant