In September 2005, TECHNOPATH opened an R&D facility and created a development plan to construct and maintain an ISO 13485 compliant manufacturing facility for the purpose of producing plasma components, quality controls, calibrators and proficiency sera for the clinical diagnostics industry. In September, 2008 we moved a custom built, GMP, manufacturing/R&D facility and in August 2009 we extended this facility to 25,000 sq feet, to incorporate customer service, logistics and distribution. In September 2009 we registered with the FDA and In March 2010, our facility became ISO13485 certification for the design and manufacture of controls and plasma components.