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.

The Veeva RIM Platform enables medical device and diagnostics manufacturers to unify systems with a single source of truth for registrations, submissions, publishing, and archival to ensure global regulatory compliance and speed to market. Through a partnership with leading data analytics company, Redica, the RIM Platform also provides a real-time regulatory information feed in the context of your product portfolio, turning data into actionable regulatory intelligence.

80%

of submission creation tasks eliminated or simplified

200+

hours saved on product approval and renewal reporting

95%

reduction in time spent on updating country records from 2 hours to 5 min

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

Keep up with a growing amount of information, adapt to the pace of change, and collaborate across the organization.

Manage Global Submissions

Author, plan, collect, and approve documents for submission to regulatory authorities in industry standard and market specific formats.

Regulatory Platform

The Veeva RIM Platform 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.

Registrations

Track product registration data, timelines, and the regulatory impact of product changes.

Submissions

Plan, author, review, and approve submissions.

Submissions Publishing

Hyperlink and validate behind-the-scenes for greater automation, transparency, and speed.

Submissions Archive

Store your complete history of regulatory submissions in the cloud.

Explore Our Regulatory Resources

View Brief

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

View eBook

RIM Buyer's Guide for Medtech

View White Paper

Evaluating Artificial Intelligence in Medtech Regulatory Affairs

View White Paper

How to Tackle Complex Medtech Regulations with Existing Resources

See All Resources

Streamline global regulatory compliance and information management

Regulatory Platform

Explore Our Regulatory Resources

Streamline global regulatory compliance
and information management