CS Analytical and Gas Testing Analytical Host Free Webinar on Gas Testing

On September 24, 2025, CS Analytical Laboratory will host a free educational webinar focused on the essential requirements for USP and EP gas testing. The event, titled “Audit Ready Gas Testing – Navigating USP, EP and FDA Requirements,” is designed to assist professionals in the pharmaceutical, biotechnology, and medical device industries in understanding and complying with regulatory standards for medical-grade gases.

Taking place at 11:00 AM EST, the one-hour session will include a Q&A segment for the final ten minutes. The webinar will be led by Chad Felter, General Manager of Gas Testing Analytical (GTA) and a seasoned expert with 15 years of experience in gas sampling and validation.

Understanding the Importance of Gas Testing

The quality and purity of gases used during the manufacturing process are critical for ensuring product safety, efficacy, and adherence to regulatory requirements. Felter emphasized that “qualification of gases used in the development and manufacturing process is an area that is often overlooked or misunderstood.” His intention is to present the webinar content in a manner that attendees can easily grasp, thus empowering them to meet their gas testing needs effectively.

Gas testing and monitoring play a vital role in maintaining manufacturing integrity, ensuring personnel safety, and fulfilling global regulatory standards. Process gases are integral throughout various stages of production, including synthesis, packaging, and storage. A rigorous validation and monitoring program, which encompasses process gases, water systems, and compressed air, is essential for complying with current Good Manufacturing Practices (cGMP).

During the webinar, participants will gain insights into how to strategically plan and implement testing protocols specific to the use of USP and EP monographed gases within their operations. This knowledge is particularly valuable for professionals in regulated industries striving to enhance their compliance efforts.

About the Hosts

CS Analytical Laboratory is recognized as the only cGMP, FDA-registered contract laboratory dedicated solely to container testing for the pharmaceutical, biotechnology, and medical device sectors. The laboratory boasts a team of experts who specialize in understanding and meeting FDA and EU regulatory expectations and USP and EP testing requirements.

In collaboration with GTA, a joint venture focused on testing, sampling, and validation of process gases and critical utilities, CS Analytical aims to help manufacturers achieve compliance with global standards efficiently. For more information about the webinar and to register, visit here.

For further inquiries or to request a quote, potential participants can visit Gas Testing Analytical’s website or contact them via email at [email protected]