Prudentia provides management and technology consulting services to the pharmaceutical and medical device industries. We advise companies on processes and technologies in support of clinical and post marketing safety and surveillance. We are experienced professionals who are passionate about drug safety and developing and implementing the right solutions for our clients. Services: • Signaling • Quality, Compliance & Performance Monitoring • SOP Planning, Implementation &Training • Audits & Inspection Readiness • Safety Database Selection & Implementation • Safety Database Migration Planning & Execution • Outsourcing Analysis & Implementation • Quality Data Management Solutions Implementation • Development of Customized tools/products in PV and Life science domain as per the client and regulatory requirements in services Why Prudentia:   • Prudentia has business and technical experience working with ARIS suite of products • Prudentia has successfully led or supported ARISg implementation and upgrade projects • Prudentia provides “one stop integrator” services for ARISg upgrades with following roles • Project Manager • E2B R3 regulatory expert • Business and Technical Analysts • Validation Lead and Analysts • Training Manager • Prudentia has the right balance of on-shore and off-shore resources to provide a cost effective team   Our Team:   • Project Managers • Technical Architects • Health Care Professionals • Strategy and Operations Analysts • Change Management Analysts • Developers • Validation Specialists • Quality Assurance Specialists  We have offices in • New Jersey, USA • Noida, India • Bangalore, India We service clients globally • USA, Europe – UK, Germany and Asia – Japan • We have an on-shore and off-shore model bringing the right cost effective team to address your needs