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Quantex Laboratories  is an independent contract testing laboratory providing a range analytical solutions to the pharmaceutical, biotechnology and medical device industries. Our capabilities and services support the entire product life cycle from research, development and manufacturing, to production, distribution and regulatory compliance.

Whether your requirements range from the out sourcing of  routine testing to the need for specialized or complex analytical studies, Quantex has  the experience and capabilities. We can perform both cGMP and GLP compliant analyses using a variety of analytical techniques including GC, HPLC, LC/MS, GC/MS, MS-MS, FT-IR, AAS, ICP and IC.  We are also capable of combining these analytical tools to provide novel approaches to product release testing, package suitability, extractables/leachables testing and GLP studies.

At Quantex, our analytical services are provided  in a timely manner with the same level of technical and regulatory standards you would expect from your own in-house laboratories. We take compliance very seriously. Our FDA registered and audited facilities are both cGMP and GLP compliant. All work performed by us is carried out under our formal QA program in conformance to cGMP and GLP requirements.

 

 
  • Method Development & Validation
  • API Impurities Identification
  • Contaminant Identification
  • In-Process Testing
  • Organic Volatile Impurities
  • Product Contamination
  • Elemental Analysis
  • Extractables and Leachables
  • Monograph Specific Analysis
  • Release Testing
  • API Impurities Profiling
  • Identification of Unknowns
  • Raw Materials Qualification
  • Residual Solvents
  • Product Off-Spec Problems
  • Trace & Heavy Metals
  • Mercury
  • Drug Metabolites

 learn more about Instruments & Equipment   Pharmaceutical Analysis Brochure

Triclosan  |  Contaminant Identification  |  Raw Materials and Specialty Chemicals |   CONEG & RoHS  |                        © 1998-2008 Quantex Laboratories, Inc.