Whitepaper
Is your facility ready for an EMPQ?
July 11, 2024 Todd McEvoy, PhD
Ensuring the safety of manufacturing pharmaceutical products relies heavily on demonstrating and maintaining control of the manufacturing environment. A well-designed environmental monitoring (EM) program allows manufacturers of both non-sterile and sterile products to observe trends in microorganism presence and to identify sources and routes of contamination. Register to download this whitepaper to…
- Understand the regulatory guidelines that need to be adhered to in order to maintain a sterile environment for product manufacturing
- Identify what factors need to be considered in order to estimate a complete timeline for an Environment Monitoring Performance Qualification (EMPQ)
- Review a list of high-level questions that need to be answered prior to performing an EMPQ
Todd McEvoy, PhD
Todd has more than 17 years of hands-on experience with complex scientific output, lab training, and management. As Senior Director of Laboratory Services, he oversees all aspects of the Lehigh Valley laboratory operations, such as developing and implementing new testing and technology, as well as training and coaching of employees. Prior to joining Azzur Labs, Todd served as general manager of an analytical laboratory specializing in method development and problem solving for the specialty chemical and polymer markets. Todd is an Association of Lab Managers (ALMA) board member and past president, as well as a Youth Association Coach for baseball, flag football, and basketball in South Parkland, PA.
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