• Laboratory Services
    • Method Development
    • Method Validation / Transfer
    • Comprehensive Analytical Release Testing
    • Stability Program
    • Reference Standard Qualification
    • Compound Characterization
    • X-Ray Powder Diffraction Analysis
    • Elemental Impurities – USP<232>, <233>, ICH Q3D
    • Nitrosamine Impurities Testing
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  • About Us
Ampac Analytical
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  • Laboratory Services
    • Method Development
    • Method Validation / Transfer
    • Comprehensive Analytical Release Testing
    • Stability Program
    • Reference Standard Qualification
    • Compound Characterization
    • X-Ray Powder Diffraction Analysis
    • Elemental Impurities – USP<232>, <233>, ICH Q3D
    • Nitrosamine Impurities Testing
  • Careers
  • Events
  • Contact Us
  • About Us

Ampac Analytical

Laboratory Services

About Us

AMPAC Analytical (AAL) supports all analytical requirements for pharmaceutical intermediates, Active Pharmaceutical Ingredients and formulated drug product. From Analytical Method Development and Implementation to Analytical Method Validation and stability, AMPAC Analytical is fully equipped with fully compliant cGMP instrumentation geared toward product analysis and product release. AAL supports spectroscopy, chromatography, particle size distribution, calorimetry, osmolality, mass spectrometry and ICH Stability project requirements.

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Contact

1100 Windfield Way
El Dorado Hills, CA 95762
916-245-6500
ampacanalytical@apfc.com

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