#USA #CS Analytical #Clifton, NJ #Gas Testing Analytical #FDA Testing

Overview of the Educational Webinar

CS Analytical Laboratory, a prominent FDA-registered contract laboratory dedicated to qualification testing, is set to host an enlightening webinar titled Audit Ready Gas Testing – Navigating USP, EP and FDA requirements. This event will take place on September 24, 2025, at 11:00 AM EST. The focus will be on meeting the essential gas testing needs in the pharmaceutical development process.

Chad Felter, General Manager of the participating company Gas Testing Analytical and a seasoned expert in gas sampling and utility validation, will lead the session. With over 15 years of experience in regulated lab operations, Chad will ensure a comprehensive overview that attendees can easily understand.

The session is designed to demystify USP and EP gas testing requirements, which are often overlooked in the pharmaceutical industry. As explained by Chad, "Qualification of gases used in the development and manufacturing process is an area that is often overlooked or misunderstood." Attendees can expect to gain the confidence needed to ensure compliance with gas testing standards.

Importance of Gas Testing in Pharmaceutical Development

In pharmaceutical, biotechnology, and medical device manufacturing, the quality and purity of utilities are critical to ensuring product safety and regulatory compliance. The potential hazards of using impure or untested gas can compromise product safety, efficacy, and lead to issues with regulatory bodies. This highlights the significance of gas testing and monitoring during production.

Process gases play a vital role throughout the production cycle—from synthesis to packaging—and require a robust validation and monitoring program. This program should encompass various utilities including gas systems, water systems, compressed air, and room air, ensuring compliance with current Good Manufacturing Practices (cGMP).

Webinar Highlights

The upcoming webinar aims to arm participants with the knowledge they need regarding the use of USP and EP monographed gases in their operations. The session will provide a detailed plan for implementing necessary testing tailored to the specific needs of individual operations.

During the one-hour event, the last 10 minutes will be dedicated to a question and answer session, allowing attendees to clarify any remaining uncertainties. This interactive segment will foster further understanding and engagement.

About CS Analytical Laboratory

CS Analytical is recognized globally as a leading cGMP, FDA-registered contract laboratory that specializes in container testing for the pharmaceutical and biotechnology sectors. This laboratory houses a team of experts well-versed in FDA and EU regulatory expectations as well as the requirements for primary package testing. Their service offerings include container closure integrity (CCI) testing, method development, validation, and analysis across various packaging components such as glass, plastic, and elastomeric materials.

As an essential partner for regulated industries, CS Analytical ensures that every product-package system meets stringent regulatory standards, which are often complex and evolving.

About Gas Testing Analytical

Gas Testing Analytical operates as a joint venture company in collaboration with CS Analytical, dedicated to specialized laboratory testing, sampling, and validation of process gases. Established by industry professionals, it helps manufacturers navigate global standards with efficiency and clarity. Individuals interested in learning more about Gas Testing Analytical or obtaining a quote can visit their website or reach out via email.

Conclusion

This educational webinar is a fantastic opportunity for professionals in the pharmaceutical industry to deepen their understanding of gas qualification testing. By attending, participants will not only enhance their knowledge but also gain practical insights into ensuring compliance with essential testing requirements. For further registration details, attendees can secure their spot at the following link: Register Here.