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CONCERNED ABOUT THE FDA's JULY 1 ISSUANCE OF NEW DRAFT GUIDANCE FOR ELEMENTAL IMPURITIES?

Quantex Laboratories 
3000 Eastpark Boulevard Suite 100
Cranbury, New Jersey  US
Phone 609-655-4047

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