Paul Daniel：Challenges in Multi-Site GxP Continue Monitorin
Paul Daniel, Senior Regulatory Compliance Expert at for Vaisala's Industrial Measurement division. Paul has eighteen years of validation experience in the pharmaceutical and medical device industries. After obtaining a Bachelor’s in biology (with honors) from the University of California at Berkeley, Paul has worked on a wide range of qualification projects, including process, cleaning, shipping, laboratory equipment, packaging, software, network, and computer validation, and extensive practical grounding in applying the good manufacturing practices principles of the FDA 21 CFR Parts 11, 210, 211, and 820, as well as a strong understanding of international GMP regulations and authoring and executing validation protocols for pharmaceutical manufacturing and software validation with a risk-based approach drawn from GAMP guidelines.
Challenges in Multi-Site GxP Continue Monitoring
Introduce different kinds of the challenges our customers may meet ,When they need to do the general continue monitoring for the Multi-site ,Multi-factory ,Multi parameter. And some different solutions for it.
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