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Our customers

Rimsys helps regulatory affairs teams of all sizes digitize and automate regulatory processes. Medtech companies, from early-stage to global leaders, rely on the Rimsys Platform to increase productivity, improve compliance, and accelerate market clearance.

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Omron
Siemens
Johnson & Johnson
Smith + Nephew
Terumo
Novartis
Avanos
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Rimsys has helped us communicate our workload and which products we need to prioritize in our region. We have 50 products on the market in the region and approximately 100 registrations. Without Rimsys it would take us a lot longer to put these reports together.
Francisco Perez
Francisco Perez
Regulatory, Quality and Customer Service

Customer stories

CASE STUDY

Omron reduces time spent on regulatory reporting by 98%

Discover how Rimsys helped Omron, a leading global medical device manufacturer of heart monitoring equipment, blood pressure monitors, digital thermometers, and nebulizers, digitize product registrations, eliminate information silos, and streamline reporting across office locations.

Omron reduces time spent on regulatory reporting by 98%
A leading global microbiology manufacturer makes regulatory information instantly accessible
A leading global microbiology manufacturer makes regulatory information instantly accessible

See how a microbiology manufacturer centralized regulatory information to give global teams to access critical information in seconds.

Global dental adhesives manufacturer reduces essential principles & GSPR maintenance by 99%
Global dental adhesives manufacturer reduces essential principles & GSPR maintenance by 99%

Discover how Rimsys helped a global manufacturer of dental adhesives and cement automate registration processes and reduce essential principles & GSPR maintenance.

A global leader in the in-vitro diagnostics market reduced time spent to create new IVDR GSPRs by 50%
A global leader in the in-vitro diagnostics market reduced time spent to create new IVDR GSPRs by 50%

See how a leader in in-vitro diagnostics digitized and automated the EU IVDR General Safety & Performance Requirements.

A global medical device manufacturer reduced release authorization workload by 88%
A global medical device manufacturer reduced release authorization workload by 88%

Discover how a $2 billion neuroendovascular technology company digitized and automated global registrations.

Rimsys gives us all the information at our fingertips in an easily searchable solution. We’ve taken a process that could take a week or a week and a half all told, and shortened it to a matter of minutes.
Global Regulatory Affairs Manager
Global Regulatory Affairs Manager
Dental Adhesives Manufacturer
Want to learn how Rimsys delivers results like these?
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Partner with Rimsys

Rimsys partners with leading medical device consultants, distributors, in-country sponsors, and technology companies.

Partner benefits include

Referrals

Opportunities to provide your complementary software and services to Rimsys customers

Revenue

Compensation for reselling the Rimsys Platform or referring leads to our team

Co-marketing

Content and event marketing opportunities to expand reach and awareness

Interested in becoming a partner?

Contact us