Modernizing MedTech Together

Unifying the Total MedTech Product Lifecycle

You focus on innovation & product development. We focus on building cloud software solutions to streamline the total product development lifecycle so you can get products to patients faster.

From ideation to commercialization, we understand the unique challenges of getting medical devices and diagnostics to market. Our cloud solutions enable medtech companies to speed clinical studies, improve quality, ensure global regulatory compliance, and streamline scientific and commercial content management.

Drive Speed Across the Total Product Lifecycle

Partnering with the industry, we continue to build unified and connected cloud software solutions across clinical, regulatory, quality, commercial, and medical affairs so you can focus on innovation and patient safety.

Clinical Data

Accelerate studies with faster builds, intuitive data capture, and monitoring with modern EDC.

Clinical Studies

Streamline end-to-end trials and improve collaboration with unified clinical operations.

Regulatory Approval

Authoritative source for global regulatory documents and information to ensure compliance.


Maximize manufacturing efficiency and product quality by unifying quality processes, content, and GxP training.

Commercial Launch

Simplify collaboration, version control, and distribution of scientific and commercial content within a global repository.

Postmarket Surveillance

Automate adverse event reporting and to accelerate continuous innovation and improve patient outcome.

Customer Stories and Testimonials

Roche Diagnostics

Lauren Buchholz shares the benefits of modernizing regulatory operations with Veeva MedTech and how Vault RIM helped them "function as global regulatory organization"

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Learn how Veeva MedTech can help you get safe and innovative products to patients faster.
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