EAG Laboratories (JA – 836)

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Audit # JA - 836
Region United States
Standards API / Excipient
Company EAG Laboratories
Location Columbia, MO USA
Date July 11th 2017
Materials The review of quality systems that support drug development services (combination of labs and GMP production areas) 1. Analytical method development and method validation 2. Stability testing and QC release 3. Impurity identification and characterization 4. Extractable and leachable testing 5. Custom synthesis 6. Radiolabeling

* If you do not have access to auditsPLUS database and would like to join this audit contact Simone Ziss at sziss@rx-360.org

* If you do not have access to auditsPLUS database and would like to license this audit contact Jaye Greene at jgreene@rx-360.org

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