The project has been divided into: PHASE 1 [months 1-12]: The final developments and innovation needed to make QUIBIM Precision a complete product; PHASE 2 [13-22] - Integrate, optimize and demonstrate QUIBIM Precision. The work has been structured in 7 Work Packages: WP1-IMAGING BIOMARKERS INNOVATION, WP2-COMPUTING PERFORMANCE AND DATA VISUALIZATION, WP3-PLATFORM INTEGRATION AND OPTIMIZATION, WP4-PRODUCT DEMONSTRATION, WP5-EXPLOTATION AND DISSEMINATION, WP6-COORDINATION AND MANAGEMENT and WP7-ETHICS REQUIREMENTS. All of these 7 WP have been completed successfully. During the first period of the project, WP1 and WP2 half of WP3 and half of the work of the transversal packages (WP5, WP6 and WP7), that extend throughout the whole project, have been carried out. During the second period of the project, WP4 and the second half of WP3 have been completed. The transversal packages (WP5, WP6 and WP7) have been extended throughout the project and closed at the end of this second phase.
The most important results achieved during SMEINST-2 regarding QUIBIM Precision product are the following: development and integration of new medical imaging analysis modules, new functionalities in the platform (i.e.: structured reporting), 3D-viewer and other visualization functionalities; optimization and High-Performance Computing; CE and ISO 13485 audits and certifications; successfully audited for GDPR compliance; FDA approval in final stage; translation of the platform, brochures, reports and website into the main languages of the EU; 2 new patents filed; marketing, communication and product dissemination in scientific and clinical environment; development of new business strategies (QUIBIM Care, QUIBIM Trials, QUIBIM Biobanks, QUIBIM Education) and reaching numerous end-users and industry thanks to pilots and customer installations, becoming a source of revenue in the coming months.