LEADING RIM SOFTWARE FOR MEDTECH 

Built for and by regulatory affairs professionals, like you

Rimsys digitizes, automates and creates regulatory order for medtech companies to ensure that products adhere to frequently changing global regulations. The only holistic RIM software for medical devices, in-vitro diagnostics, and medical device software, Rimsys makes it easy to manage global UDI requirements and navigate the pillars of regulatory affairs, including product registration, standards management, essential principles/GSPR.

 

Join leading medtech companies, like Johnson & Johnson, Siemens Healthineers, and Terumo, using Rimsys to simplify and streamline regulatory information management. Schedule your personalized demo of Rimsys today. 

Attending RAPS Convergence 2021? Stop by our virtual booth 9/13-9/15 for giveaways, networking and more!

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Trusted by World-Leading MedTech Companies

NAVIGATE THE PILLARS OF REGULATORY AFFAIRS EASILY

Rimsys is the only holistic RIM software on the market designed specifically for medical technology companies, with functionality for the pillars of regulatory affairs.

Product Registration

Monitor and manage global registrations and regulatory applications.

Essential Principles

Digitally create, manage, and maintain all Essential Principles.

Standards Management

Automatically and proactively monitor and manage global standards.

Regulatory Intelligence

Track changing laws, regulations, guidance documents, and relevant news.

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FAST, EASY, AND SECURE IMPLEMENTATION

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100% cloud-based

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Product-centric

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Easy enterprise integrations

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Secure and compliant*

*Compliant to: FDA 21 CFR Part 11, ISO 27001, ISO 9001 and AICPA/SOC

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Used and trusted by the world’s leading medtech companies

Our platform is used and trusted by companies, including Johnson & Johnson, Siemens Healthineers, and Terumo, because it consolidates all the functions of regulatory affairs, making it easy for you to digitize, automate, and navigate the global regulatory landscape.

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Built by and for regulatory affairs professionals in medtech

Rimsys was built by regulatory affairs professionals who spent decades dealing with the same inefficiencies you experience today. We carefully designed an interface to mirror the workflows you know and developed secure archives to provide your company with continuity over time.

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Easy to start and simple to scale as your company grows

Rimsys creates efficiencies in your department so you can focus on the job you were hired for. As completely off-the-shelf software, Rimsys is fast and easy to implement, and maintenance-free.

WHAT LEADING COMPANIES ARE SAYING

“No alternative even comes close to Rimsys.”

– Jose, RA Manager at a world-leading blood pressure monitoring manufacturer

“If you’re a medical device regulatory professional…. I promise you, [Rimsys] will change your life in a good way.”

– Jon Speer, Founder at Greenlight Guru

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READY TO DEMO RIMSYS?

Schedule your demo now to learn how Rimsys consolidates all the functions of regulatory affairs, making it easy for you to digitize, automate, and navigate the global regulatory landscape.

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ABOUT RIMSYS

Rimsys is a world-leading Regulatory Information Management software for medical technology companies that digitizes, automates, and creates regulatory order. The only holistic RIM software for medical devices, in vitro diagnostics, and medical device software, Rimsys makes it easy to navigate the pillars of regulatory affairs, including product registration, standards management, essential principles/GSPR, and regulatory intelligence. Rimsys is a holistic platform built by and for regulatory affairs professionals to efficiently ensure that products adhere to changing global regulations.