Analytical Procedures and Methods Validation EU
June 21 - 23, 2016 - Dublin MA USIVT Network
sabrina.delio@cbinet.com
Phone:339-298-2285
In 2015, FDA released their final guidance on APMV, an update to the Agency’s current requirements for regulatory submissions of analytical procedures and method validation data. The intention of this guidance is to support the documentation of the identity, strength, quality, purity and potency of drug substances and drug products. IVT’s Analytical Procedures and Methods Validation EU is the industry’s leading forum on global regulatory trends and provides the tools needed to excel in daily core responsibilities in a highly regulated environment.
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