We’re on a mission to digitize, automate, and create regulatory order for the medical technology industry.Join the team
Rimsys was founded in 2017 by regulatory affairs professionals who asked the simple question: “Isn’t there a better way to do this?” Like all RA teams, they spent hours looking for information, manually managed global product registrations, and struggled to keep up with changing regulations and standards. The Rimsys Platform is designed specifically to help medtech companies address these challenges, and confidently establish global regulatory compliance.
The EU MDR/IVDR rollout is the first of what promises to be many major shifts in the global regulatory landscape. Manually managing products, registrations, standards, and selling status in large color-coded spreadsheets won’t keep pace. Hiring external consultants for administrative work isn’t cost effective. Rimsys centralizes regulatory information and automates processes to increase RA productivity, manage complexity, and reduce compliance risks.
We empathize with our customers and continuously innovate our product to create an extraordinary customer experience
We continually acquire, adapt, and grow our professional and industry knowledge
We are change agents and are accountable to our customers and team members in achieving excellence
We foster a nurturing, diverse, inclusive, passionate, and enabled workforce