Posted October 16, 2013 by Nicole Belanger
MicroGroup Process Validation Plan is a Key Tool to Risk Management
MicroGroup, Inc., of Boston, MA and Twin Cities, MN continues to enhance its value to OEMs in the medical, aerospace and other markets with the advancement of its suite of quality management capabilities and tools – particularly its robust Process Validation Master Plan. Where patient safety and risk aversion are critical concerns to OEMs, MicroGroup’s Process Validation Plan establishes documented evidence to provide a high degree of assurance that a specific process will consistently produce to the pre-determined specifications and quality attributes. Moreover, MicroGroup’s plan helps speed up the regulatory and production timelines, improving a product’s time-to-market
- As part of its Quality Management System, MicroGroup’s First Article Inspection capabilities of new components shortens the production process
- MicroGroup’s Process Validation Plan includes Installation Qualification (IQ), Operational Qualification (OQ), and Process Performance Qualification (PQ)
- MicroGroup is executing against its comprehensive, detailed Validation Master Plan
Said William Bergen, President and CEO of MicroGroup, Inc., “Our expertise in process validation, a key focus area for many of our customers, is consistent with our focus on Speed and Precision. Our efforts in this area allow our customers to be confident that the components and assemblies they receive from us, from prototype through commercial quantities, are of the highest quality.”
MicroGroup welcomes all OEMs to send a print, CAD file or concept drawing of a development project to firstname.lastname@example.org for a complementary production assessment and a price proposal.