Streamline global regulatory compliance and information management

Globalization, supply chain complexity, patient safety, and new regulations are significantly impacting the total product lifecycle. Managing global compliance can involve more than 100 different systems and spreadsheets, often resulting in manual, cumbersome processes and a slower time to market.

Veeva MedTech enables medical device and diagnostics manufacturers to unify systems with a single source of truth for registrations management, submissions, and publishing to ensure global regulatory compliance and speed to market.

Real-time Submissions and Registrations Visibility
Facilitate better access, visibility, and control over regulatory documents, data, and processes in real-time.
Track Global Registrations
Track and understand the status of your registrations across the globe and view KPIs in real-time to stay proactive.
Ensure Compliance
Mismanaged process can lead to financial penalties, product delays, and a tarnished reputation. Advanced RIM solutions enable you to keep up with a growing amount of information, quicken the pace of change, and collaborate more.
Manage Global Submissions
Author, plan, collect, and approve documents for submission to regulatory authorities in industry standard and market specific formats.

Regulatory Suite

The RIM Suite is a unified group of cloud software applications that provides end-to-end visibility, oversight, and control for all regulatory compliance documents, data, and Health Authority correspondence, throughout the total product development lifecycle.

Track product registration data, timelines, and regulatory impact of product changes.
Plan, author, review, and approve submissions.
Cross-document hyperlinking and validations behind-the-scenes for greater automation, transparency, and speed.
Store your complete history of regulatory submissions in the cloud.

Explore Our Regulatory Resources

Image for Unified RIM application for end-to-end regulatory compliance management
View Brief

Unified RIM application for end-to-end regulatory compliance management

Image for Modernizing Regulatory Affairs: 2021 Regulatory Benchmark Report
View Report

Modernizing Regulatory Affairs: 2021 Regulatory Benchmark Report

Image for GE Healthcare: Seven KPIs to Measure RIM
View Blog

GE Healthcare: Seven KPIs to Measure RIM

Image for Alcon and Terumo share key areas where digitalization can support global compliance
View Webinar

Alcon and Terumo share key areas where digitalization can support global compliance

Learn how Veeva MedTech can help you get compliant, quality products to patients faster.
Contact Us