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.

Registrations

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

Submissions

Plan, author, review, and approve submissions.

Submissions Publishing

Cross-document hyperlinking and validations behind-the-scenes for greater automation, transparency, and speed.

Submissions Archive

Store your complete history of regulatory submissions in the cloud.