PITTSBURGH, October 6, 2015 — Gateway Analytical announced today that they will be exhibiting at the 7th Annual Pharmaceutical and Medical Device Manufacturing and Quality Operations Forum in New Orleans, Louisiana, October 8-9th. This forum meeting brings together executives from throughout the pharmaceutical and medical device industries to discuss the key challenges faced by manufacturers, and to explore innovative strategies and solutions for addressing the increasing challenges faced by the industry.
During the conference, Gateway Analytical will be promoting medical device testing services that focus on supporting product quality issues such as analyzing wear debris, materials characterization, lifecycle sustainability and failure analysis. “This will be our first year exhibiting at the Annual Pharmaceutical and Medical Device Manufacturing and Quality Operations Forum, and we are looking forward to participating in the discussions regarding the critical challenges this industry faces when it comes to developing and maintaining medical device product quality,” said David Exline, Senior Vice President at Gateway Analytical. “We know there are many stages to a product’s life cycle and our testing capabilities can help support manufacturers throughout their entire process, even when it comes to instances of determining the source of product failures for recalls.”
Gateway Analytical is a full service, cGMP compliant, ISO 17025:2005 certified, DEA licensed and FDA registered and inspected laboratory with specialized expertise in techniques for chemically specific analysis and particulate contamination identification. For more information on Gateway Analytical medical device testing services, contact Karen Sutch, Business Development Manager at 724-787-7702 or email@example.com.