Regulatory Automation & Compliance Improvement
DXC RIM.AI helps you accelerate regulatory submissions for new therapies, devices and medicines in global markets. FirstPoint RIM.AI product suite is used by 500+ clients globally for their regulatory submissions. To cite just a couple of examples, among our clients we have seen zero refusal to file (RTF) for on-time, within budget submissions, and15% productivity gains on IND/NDA application compilation, submission and regulatory approvals. With our Total Regulatory Solution Suite, you can simultaneously publish and submit new drug applications in multiple markets and in compliance with a variety of regulatory formats, saving time and increasing productivity.