Powerful, straightforward RIM solution.
The value of complete visibility on content progress during authoring and review, as well as understanding submission life cycle is critical to regulatory affairs and operations.
Compliance meets Collaboration
Part 11 compliance provides a fully validated environment. By marrying compliance-centric features to collaboration and management features, your organization will rock efficiency.
Built for
Distributed Teams
You rely on multiple partners, contractors, and colleagues distributed globally to make things happen. Good news, Kivo was built for this. You can securely manage all types of users and authentication.
Land and Expand
Kivo offers class-leading RIM functionality, and adding eTMF and Quality Management features expands Kivo utility throughout the drug development process. We are built to support exactly how you run your business.
Goldilocks Mix of Regulatory Features
Kivo is focused on only the features that matter to your business, such as seamless hand-offs to regulatory publishing groups and visibility into source documents included in any submission.
Welcome to the intuitive platform that will change the way you work.
When you partner with Kivo, you get the keys to power, speed, and control:
- Ensure data integrity with an immutable audit trail
- Improve regulatory sustainability
- Build documents in a fraction of the time
- Iterate without compromising security