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Better results. Faster. As soon as your sample comes through the door, we spring into action to properly log it, store it, and notify the individual scientists that will be diligently working on your project. Then it's off to specialized sample preparation and analytical probing by our fleet of cutting edge instruments. You'll have data, interpretation, and solutions in no time.
Gateway Analytical has carefully assembled a diverse team of curious experts. When the other guys run away from difficult problems or second guess their approach, our scientists move in to take a closer look with a forensic-based framework. Our process is focused on outcomes and driven by experts that have seen it all. You bring challenges. We deliver creative solutions.
We're not just another analytical lab. Why not? We spent years building a leading position in the highly-regulated pharmaceutical industry. That means our facilities are FDA-inspected, cGMP certified, and maintain ISO 9001 (quality management) and ISO 17025 (testing and calibration) standards. Simply put, there's a high bar for quality in all our work that others just can't match.
When you need us, call us. We're always here to answer your questions. As our growing list of returning customers has learned, you'll get to know the individual scientists working with your team to deliver results. They're real people. Our innovative real-time collaboration technology even allows us to demonstrate results and provide updates -- live from the lab.
See the latest technical contributions from our expert team.
The overall objective of a solid quality foundation in the evaluation of particle contamination analysis of inhalables is based on many things. The complete evaluation and root cause analysis of foreign particulate matter, as well as the affects of particulate on product quality, are essential when evaluating the processes for developing and implementing an inhalable product. In addition, a methodology for determining acceptable limits and methods for ensuring product quality must be evaluated early on in the development process to ensure the best end product. Finally, the analytical methods utilized to test particulate and determine the particulate source are critical in the success of any testing program.
This webinar was designed for individuals involved in the manufacturing of inhalable drug products, including quality control, optical inspection and process development/engineering personnel. During this webinar, our presenter provided examples of commonly found contaminants in inhalable drug products and how these contaminants are introduced into the manufacturing process. He presented to the audience a basic multi-tiered analytical approach to characterize foreign particulate matter and how to solve particulate contamination issues in inhalable drug products using a scientific approach. The importance of taking a pro-active approach to quickly source and manage contaminant issues in the manufacturing process to reduce the risk of future contamination was also discussed.
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If we’re not in the lab you can find us presenting or mingling at industry events across the globe. Interested in meeting up? Contact us to make arrangements!
