Cary, NC (PRWEB) January 30, 2014
InstantGMP, Inc. has been providing software solutions to effectively manage FDA/cGMP compliance for over 10 years. Now they are building on that experience and are excited to be starting Beta testing of a new version designed specifically for Medical Device Manufacturers to help them manage their Quality System Regulations compliance.
InstantGMP™ QSR is a cloud based manufacturing software that can make producing medical devices easier. In order to know for sure that it has everything medical device manufacturers will need, they are looking for some companies to participate in beta testing and to give some feedback.
InstantGMP™ QSR is based on the InstantGMP MES manufacturing execution system that has been used for producing pharmaceutical products since 2004. InstantGMP, Inc. would like to learn if medical device companies would experience similar benefits by using an electronic manufacturing system that can easily organize and track Master Device Records and Design History Files. They plan to complete the Beta testing phase and launch a completely vetted and validated product in Q2, 2014.
About InstantGMP, Inc.
InstantGMP, Inc. develops web-based software for manufacturing products that must comply with current Good Manufacturing Practices (cGMP) and FDA requirements. Our software systems were developed to meet the standards of cGMP, GAMP and 21 CFR Part 11. InstantGMP™ MES is a manufacturing execution system and InstantGMP™ EBR is an electronic batch record system. These software systems were designed to include the quality and cGMP checks necessary to make manufacturing cGMP products easy.