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Founded in 1997, Global Technical Partners provides FDA-regulated industries solutions to address the software, hardware, and process requirements of cGMP, GLP, and Part 11 including electronic records managment, electronic signatures, electronic passwords, audit trail, and validation. GTP, as a
consulting company to some of North America's premier pharmaceutical,
biotech, and medical device manufacturers, has been immersed in a series of multi-year, multi-million dollar projects.
Our mission is to provide
star-quality services and solutions to the manufacturing marketplace, with a
particular emphasis on companies implementing ERP systems, Quality Applications (LIMS, Chromtography, Change Control, Document Management) and Clinical Applications.
GTP's consultants draw upon their considerable expertise in technology, their understanding of regulatory requirements, their in-depth knowledge of the
packaged software that they service, and their understanding of real-world
business IT requirements.
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