Mission3 leverages its in-depth expertise of technology in the life sciences industry to provide premier regulatory information management systems to companies of all sizes and segments. By combining highly intuitive products with value-added services, we enable our clients to achieve their commercial goals in markets worldwide.

Simplicity
Our software is fundamentally designed keeping end users in mind. All of our products are web-based, require no desktop licenses and are highly configurable which makes them very adaptable to changes in the business, and therefore less costly to maintain as well.

Inclusive
We specialize in providing fully integrated solutions. Not only do our products integrate with each other, they also have the ability to align with existing information systems. We believe strongly in breaking down the "silos" of people and information that so often impede the very processes they are intended to enhance. Our open product platform recognizes your existing investments and works seamlessly with them.

Customer Value
We use our knowledge and expertise of technology and the industry to deliver the best solutions to you. Our platform will significantly enhance your organization's productivity, lower operational costs and shorten time-to-market.

Mission3 Capabilities

• Multi-user platform for content creation, management and approval. 21 CFR Part 11 compliant.
• Due diligence solution for secure, 24x7 access to information for external review.
• Submissions assembly and publishing, eCTD, 510k, PMA, Study Reports.
• Project management tools for associating timelines, resources and tasks with content.
• Tracking registration statuses and correspondence globally across your existing systems. Integrating Business Intelligence (BI) and Business Process Management (BPM) with your existing systems.

Mission3 Advantages

• Plug-and-play, web-based and 100 percent configurable, rapid deployment for small as well as large firms.
• Project-based pricing, no upfront licensing or hardware costs.
• Automate tracking/reporting of critical project progress metrics across multiple repositories.
• Single-source your content and reporting needs, reduce implementation and validation costs.
• Comply with global regulations – eCTD, PMA, 510k out-of-the-box.