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On September 24, 2025, CS Analytical Laboratory will host an educational webinar titled “Audit Ready Gas Testing – Navigating USP, EP and FDA requirements.” The event aims to provide a thorough overview of gas testing requirements as outlined by the United States Pharmacopeia (USP) and the European Pharmacopeia (EP). This initiative is particularly relevant for professionals in the pharmaceutical development process.
Webinar Details and Expert Insights
The webinar is scheduled for 11:00 AM EST and will last one hour, concluding with a 10-minute Q&A session. Registration is free and can be completed through the following link: CS Analytical.
Chad Felter, General Manager of Gas Testing Analytical, will lead the session. With over 15 years of experience in gas sampling, utility validation, and regulated laboratory operations, Felter aims to demystify the often-overlooked aspects of gas qualification. “Qualification of gases used in the development and manufacturing process is an area that is often misunderstood,” Felter stated. He emphasized the importance of providing a comprehensive overview of the relevant requirements to help attendees feel confident in their gas testing capabilities.
The Importance of Gas Testing in Regulated Industries
In the realms of pharmaceutical, biotechnology, and medical device manufacturing, ensuring the quality and purity of process utilities is vital for product safety and regulatory compliance. Gas testing plays a crucial role in maintaining manufacturing integrity and safeguarding personnel. Process gases are integral throughout the production cycle, from synthesis to packaging and storage.
A robust validation and monitoring program that covers process gases, water systems, compressed air, and room air is essential for operations compliant with current Good Manufacturing Practices (cGMP). Webinar participants will gain significant insights into effectively planning and implementing testing specific to the use of USP and EP monographed gases within their internal operations.
Established as the world’s only cGMP, FDA-registered contract laboratory exclusively dedicated to container testing, CS Analytical specializes in meeting the regulatory needs for the pharmaceutical, biotechnology, and medical device industries. Their team consists of leading experts in regulatory expectations, particularly concerning USP and EP primary package testing, including container closure integrity testing.
As a joint venture with Gas Testing Analytical, this collaboration aims to equip regulated manufacturers with the necessary tools and knowledge to meet global standards efficiently. For further information or to request a quote, interested parties can visit Gas Testing Analytical or email [email protected].
This upcoming webinar represents an opportunity for industry professionals to enhance their understanding of critical gas testing requirements, making it a valuable resource in the ever-evolving landscape of pharmaceutical development.
