Please join us for a free webinar on March 26th, at 1 p.m. Eastern Standard Time, exploring the testing options for Disinfectant Efficacy Testing on Site-Specific Surfaces.
Bodies like the FDA demand a more rigorous validation of cleanroom disinfectants, going beyond what the EPA registration tests cover. This session is designed to equip you with critical regulatory knowledge and actionable advice, ensuring that your procedures align with the current Good Manufacturing Practices and navigate this complicated regulatory landscape.
By joining us, you'll gain insights into:
- Additional layers of validation required by agencies like the FDA.
- Practical strategies to ensure your disinfectants are both effective and compliant.
- Principles presented in USP <1072> Disinfectants and Antiseptics.
- How to confidently adhere to the stringent standards in your industry.
This webinar is intended for anyone involved with the adherence to cGMPs, as well as those involved in quality assurance of a Pharmacopeial article manufacturing or processing facility in relation to aseptic processing.
Presented by: Grady Wertman, Study Director III
Grady has worked at Nelson Laboratories Bozeman for over 10 years. He started as a laboratory technician and quickly found a passion in working with customers and designing evaluations that fit their intended goals. His expertise lies in bridging the gap between technical proficiency and customer satisfaction, ensuring that each project meets the highest standards of quality and efficacy.
