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    • Elemental Impurities Testing and Analysis
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  • Laboratory Services
    • Compound Characterization
    • Comprehensive Analytical Release Testing
    • Elemental Impurities Testing and Analysis
    • Extractables and Leachables
    • Method Development
    • Method Validation / Transfer
    • Nitrosamine Impurities Testing
    • Reference Standard Qualification
    • Stability Program
    • X-Ray Diffraction Analysis
  • Resources
    • Events
    • Webinars and Brochures
    • Analysis Blog
    • Press Releases
    • Careers
    • Sample Submissions Form
    • Shipping Requirements
    • Request A Quote
    • Terms and Conditions
  • Contact Us
  • About Us
    • Privacy Policy
    • Cookie Policy

Ampac Analytical

ICP-MS

March 13, 20232850 × 2625Elemental Impurities
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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