Gateway Analytical announced today that they will be exhibiting at the annual Eastern Analytical Symposium and Exposition (EAS) in Somerset, New Jersey on November 17th and 18th. EAS is held each year to provide professional scientists and students continuing education in the analytical and allied sciences through the presentation of symposia of papers, workshops, and short courses. An exposition of apparatus and supplies allied to these sciences is held concurrently with the symposia.
During the conference, Gateway Analytical will be promoting a wide array of analytical testing services that focus on supporting pharmaceutical drug manufacturing quality control including particulate contamination identification, root cause analysis, glass delamination analysis, deviation, and out-of-specification investigation support. Of particular interest to conference attendees is Gateway Analytical’s ability to give preliminary results in as little as 24 hours with a final analytical report available in 48 hours in some cases.
“We recognize that manufactures often need analytical support at many different levels and with our wide range of technology and expertise in both common and specialized areas such as foreign particulate identification and glass delamination analysis; Gateway Analytical is in a good position to be able to support drug manufactures throughout their entire process,” said Dave Exline, Senior Vice President at Gateway Analytical.
Gateway Analytical is a full service, cGMP compliant, DEA licensed, FDA registered and inspected laboratory with specialized expertise in techniques for chemically specific analysis and particulate contamination identification. For more information on Gateway Analytical’s pharmaceutical investigation services, visit booth #235 while at the EAS Expo or contact Paige Cohen, Sales Development Associate, at 724-442-1900 x 129
