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 Clinical Basics
Clinical Basics: eTMF is a cloud-based electronic trial master file system that enables organizations to efficiently manage their clinical trials. With full support for the latest version of the TMF Reference Model, Clinical Basics: eTMF gives sponsors and CROs real-time access to clinical documentation at every point in a trial’s set-up, execution, and archival.
Clinical Basics: CTMS gives you the ability to track and manage your clinical trial operations end-to-end, including study management, study monitoring, and issue management.
Veeva Quality Basics
Quality Basics: QMS provides a preconfigured environment for managing changes to and deviations from established quality processes.
Quality Basics: QualityDocs provides a preconfigured environment for GxP quality content management.
Quality Basics: Training is a preconfigured Learning Management System (LMS) designed for GxP compliance. It provides tools to manage learning content and curricula and to deliver and track assignments.
Veeva LearnGxP is a comprehensive training solution that helps life sciences companies ensure regulatory compliance and stay inspection-ready at every stage. This subscription-based service offers a large variety of pre-built content across GxP (such as GMP, GCP, GLP, GVP, GDP, GDocP), Corporate Compliance, and Environmental Healthy & Safety. Our courses provide a modernized and holistic approach to compliance training, making it easy and convenient for companies to stay up-to-date with regulations.
LIMS Basics is a laboratory information management system used for Quality Control (QC) testing of a manufactured product.
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.
Veeva Commercial Basics
PromoMats Basics provides an end-to-end solution for managing promotional materials. It helps organizations streamline the complex process of creating, reviewing, approving, distributing, and maintaining compliant content for Pharma, Biotech, and Medtech.