CS Analytical Laboratory, a leading FDA-registered contract laboratory, is set to host an informative webinar titled “Audit Ready Gas Testing – Navigating USP, EP and FDA Requirements.” This free event, in partnership with Gas Testing Analytical, aims to provide participants with a thorough understanding of gas testing protocols essential for pharmaceutical development. The webinar is scheduled for September 24, 2025, at 11:00 AM EST and will last for one hour, concluding with a Q&A session.
Chad Felter, General Manager of Gas Testing Analytical and a seasoned expert with 15 years of experience in gas sampling and utility validation, will lead the session. Felter emphasized the importance of understanding the qualification of gases used in manufacturing processes, stating, “Qualification of gases used in the development and manufacturing process is an area that is often overlooked or misunderstood.” He aims to simplify the complex requirements of the United States Pharmacopeia (USP) and European Pharmacopeia (EP) for attendees.
Maintaining the quality and purity of process utilities is crucial in the pharmaceutical, biotechnology, and medical device sectors. Gas testing plays a vital role in ensuring product safety, efficacy, and adherence to regulatory standards. Process gases are integral throughout various stages of production, from synthesis to packaging and storage. As such, a comprehensive validation and monitoring program is essential for operations that comply with current Good Manufacturing Practices (cGMP).
Webinar Insights and Registration Information
Participants in the webinar can expect to gain valuable insights into best practices for testing USP and EP monographed gases in their operations. The session will cover key regulatory requirements and provide actionable strategies for ensuring compliance.
The webinar is complimentary, and interested attendees can register online at the following link: Register for the Webinar.
About CS Analytical Laboratory:
Founded to serve the pharmaceutical, biotechnology, and medical device industries, CS Analytical Laboratory is the only cGMP, FDA-registered contract laboratory focused on container testing. The laboratory team consists of industry-leading experts knowledgeable in FDA and EU regulatory expectations, as well as USP and EP primary package testing requirements including container closure integrity testing. Their services encompass CCI method development, validation, and analysis, physical and physicochemical testing, and a range of complementary services for various primary packaging materials.
About Gas Testing Analytical:
As a joint venture with CS Analytical, Gas Testing Analytical specializes in the testing, sampling, and validation of process gases and critical utilities. Established by industry experts, GTA is dedicated to helping regulated manufacturers meet global standards with efficiency and clarity. For more information or to request a quote, visit Gas Testing Analytical or contact them via email at [email protected].
This webinar represents an important opportunity for professionals in regulated industries to enhance their understanding of gas testing requirements and ensure compliance with the latest regulatory standards.
