A New Frame Work for Integrating Standard Operating Procedures With a Cloud Based Manufacturing Software for Medical Devices Announced

InstantGMP developed a cloud based manufacturing software system for cGMP production of medical devices with the requirements from Standard Operating Procedures integrated into the software.

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Medical Device Manufacturing Software

Cary, NC (PRWEB) March 04, 2014

InstantGMP QSR is a new software system for manufacturing medical devices that introduces an innovation for complying with the standard operating procedures (SOPs) required by the FDA's Quality System Regulation (QSR).

Today, more than ever, innovation is critical to maintaining compliance with FDA requirements and being competitive. By integrating SOP requirements into the software, InstantGMP QSR was created in a unique way so medical device manufacturers can meet both these challenges.

Any quality system, which a collection of SOPs and Policies, is a critical tool for assuring that products are made consistently and customers can trust what they get from their suppliers. InstantGMP makes available a full set of manufacturing SOPs designed to work in coordination with existing SOPs and legacy quality systems and with their medical device manufacturing software. These SOPs are written to allow them to be entered into a current quality system with little effort. Since the requirements of these SOPs are built into InstantGMP™ QSR, implementation and training is easy.

About InstantGMP
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 manufacturing cGMP products easy.


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