Our eSTAR interface is changing the game on FDA 510(k) submissions

Our eSTAR interface is changing the game on FDA 510(k) submissions

Our eSTAR interface is changing the game on FDA 510(k) submissions

Our eSTAR interface is changing the game on FDA 510(k) submissions

Easily manage global registrations of medical devices

Start managing global registrations with advanced and innovative technology. With Essenvia, you no longer need to use color-coded spreadsheets to manage device registrations.

TRUSTED BY INNOVATIVE MEDTECH COMPANIES WORLDWIDE

TRUSTED BY INNOVATIVE
MEDTECH COMPANIES WORLDWIDE

How can the Essenvia RIM Platform help you manage your global product registrations?

Global Registrations

Manage product registration lifecycle by country.

Centralized Information

Central repository for all registration documents
linked to product master data.

Friendly Dashboards

Dashboard to track and monitor your registration status
across multiple geographies and countries.

Easy Integration

Integration to ERP/PLM for product data
and registration document synchronization.

Why use a Regulatory (RIM) Platform to manage Product Registrations?
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Learn more about the Essenvia RIM Platform

Contact us for a Demo

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Learn more about the Essenvia RIM Platform

Contact us for a Demo