Veeva Basics is a preconfigured and prevalidated product offering specifically addressing the needs of emerging small-market biotech companies who are preclinical or preparing for their first clinical trials. In addition to the software itself, Veeva Basics includes support, release management, validation, training, and standard operating procedures (SOPs).
Veeva Basics Key Features
Veeva Basics is delivered fully configured and includes the following key features:
- Veeva Basics is preconfigured using the industry’s best practices, and are simpler than full Vault installations.
- Every instance of a Veeva Basics application is guaranteed to have the same configuration.
- Veeva Basics is not configurable. The configuration is not editable by customers or by Veeva support. All configuration updates follow the engineering build process and are validated before release.
- Veeva Basics can be upgraded to full Vault, which enables the full Vault configuration and functionality. Upgraded Vaults no longer receive Veeva Basics updates.
Veeva RIM Basics
Veeva RIM Basics provides an end-to-end solution for managing regulatory submissions. It helps organizations streamline the complex process of preparing, managing, submitting, and maintaining regulatory documentation required by global health authorities.
Veeva RIM Basics provides the following benefits:
- Provides a single source of truth for tracking the progress of regulatory submissions globally.
- Includes purpose-built tools optimized for regulatory processes.
- Facilitates compliance with global and regional regulatory requirements.
- Allows easier collaboration and insight into submission progress.