Validation refers to establishing documented evidence that a process or system, when operated within established parameters, can perform effectively and reproducibly to produce a medicinal product meeting its predetermined specifications and quality attributes
Monday, January 1, 2018
Analyzing the FDA Process Validation Guidance
The US Food and Drug Administration's "Process Validation: General Principles and Practices" is now over three years old. Thus, it is shocking how many pharmaceutical and medical device manufacturers have not implemented the approach suggested in this guidance. In this presentation, Paul Pluta, Ph.D., analyzed and clarified the FDA process validation recommendations.
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