Bringing 25 Years of Regulatory Expertise to Every Team—with a Powerful Suite of AI Tools

May 19, 2025

At Quroba, we are building something designed to change how teams in medtech, biotech, and digital health approach regulatory and quality work. For too long, navigating compliance has been slow, complicated, and costly—especially for innovators trying to move quickly. We believe AI can change that.

Drawing on decades of hands-on experience—including 25 years of regulatory knowledge from our partner Kwame Ulmer, a former FDA reviewer we are creating tools that make it easier for teams to understand where they are, what they need, and how to move forward confidently. What once required weeks of back-and-forth or high-stakes guesswork can now be simplified with intelligent systems trained by experts who have seen it all.

AI is not just hype it is already starting to reshape life sciences. McKinsey estimates it could unlock over $100 billion in value annually for the industry, largely by cutting down inefficiencies and speeding up critical paths like regulatory approval and documentation. For teams buried in complexity, it is a chance to streamline the process, reduce risk, and stay focused on innovation.

We have built something we are excited about—and we are ready for others to try it. If you're facing regulatory hurdles or looking to modernize your approach to quality and compliance, contact us below to get early access and experience what Quroba's AI Regulatory Chatbot can do.