Smooth your drug development and commercialization process with laboratory services designed with your objectives in mind.

Leverage our well-equipped state-of-the-art facilities to handle your projects of any size, scope or complexity.

  • Analytical Development & Validation
  • Residual Solvents
  • Elemental Impurities
  • Extractables & Leachables
  • Drug Release/Dissolution
  • Full Monograph Testing per USP, EP, BP, JP, FCC, ACS, AOAC, AOCS
  • Method Verification & Transfer
  • Quality Control & Release Testing
  • Trace & Heavy Metals
  • Stability & Shelf-Life Testing
  • Impurity Profiling

FDA Registered and Inspected  • ISO/IEC 17025:2005 Accredited  • Held to the world's highest standards

Quantex provides a comprehensive suite of analytical and testing capabilities in support of FDA-regulated industries. Contact us to request a quote on your next project.

Contact Tim Hennessey by email or by phone at 609.655.4047 x304.

CONCERNED ABOUT THE FDA's JULY 1 ISSUANCE OF NEW DRAFT GUIDANCE FOR ELEMENTAL IMPURITIES?
Click here to read Quantex Labs CEO Dr. James Menoutis's thoughtful approach on Elemental Impurities and the USP's revised standards.
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Quantex Laboratories 
3000 Eastpark Boulevard Suite 100
Cranbury, New Jersey  US
Phone 609-655-4047

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