Cary, NC (PRWEB) April 01, 2014
InstantGMP, Inc., the manufacturing software company that pioneered accessible, easy-to-use electronic batch record software for products manufactured using Good Manufacturing Practices (GMP) has just completed development of a report generator for their Manufacturing Execution System software. InstantGMP MES is the first cloud-based system created specifically for use in manufacturing FDA-regulated products. It will now provide the benefits of controlled documentation and GMP-regulated queries without any IT overhead or need for regulatory experts.
"We were hit immediately by three key findings when our discussion with FDA-regulated manufacturers began," says Dr. Richard Soltero, President and founder of InstantGMP. "They are all extremely passionate about their product quality. And they're business people first; they see GMP as a gold standard that can help them maintain their customers' loyalty. Finally, the industry really understands the concept of building quality into their processes and applies the principals of GMP throughout."
"With a report generator function now available," Dr. Soltero continues, "GMP product makers now have an electronic manufacturing platform that efficiently automates standard reporting for any number of queries with a set of pre-configured reports that can locate specific lots or batches, or report stock levels and restock requirements. The system can also be enhanced with customized reports that individual specific needs. Manufacturing FDA-regulated product using best practices is easy to achieve with InstantGMP™ MES."
InstantGMP, Inc. develops web-based software for manufacturing products that must comply with current Good Manufacturing Practices (cGMP) and FDA requirements. These software systems were developed to meet the standards of cGMP, GAMP and 21 CFR Part 11. They were designed to include the quality and cGMP checks necessary to make products with good manufacturing practices easy.