Quality, Regulatory, Clinical, and Commercial Software for Emerging Biotechs

Veeva QualityDocs Basics is the industry-leading regulated quality content management solution. Including best practices for managing SOPs and other regulated content.

Veeva Training Basics is an industry-specific LMS ensuring that your team is ready to perform their jobs while enabling GxP compliance and audit readiness.

Veeva QMS Basics enables seamless management and tracking of quality processes. Includes Audits, Change Control, Deviations, and Standalone CAPA.

Veeva LIMS Basics empowers virtual life science companies to digitize and scale their QC data. It centralizes specifications and external testing results for consistent data, compliance, and accelerated batch release.

LearnGxP is a specialized, industry-focused library of accredited GxP training, providing a seamless way to train your team and maintain ongoing compliance.

Browse our catalog of training content that is relevant to emerging biotech companies.

Veeva Submissions Basics is used to plan, collaboratively author, review, and approve regulatory documents. It includes dashboards and reports to allow submission managers to track the status of documents in real time.

Veeva Submissions Archive Basics is a secure repository of submission-published output and includes a viewer for easy access to historical applications submitted to health authorities.

Veeva Submissions Publishing Basics streamlines the assembly, formatting, and publishing of regulatory submissions, ensuring compliance with health authority requirements.

Veeva eTMF Basics is the leading trial master file application used to ensure quality, timeliness, and completeness of a TMF. It provides full content management capabilities for upload, version control, QC/approval, and real-time co-authoring for study documents.

Veeva CTMS Basics allows for more complete management of your trials including Study Milestones, Monitoring, Subject Enrollment, Issue Management, and Site Communication Tracking.

Veeva MedComms Basics is a unified source of truth for medical content. It streamlines the creation, approval, and distribution of scientific materials, ensuring Medical Affairs teams deliver consistent, compliant responses globally.

Veeva CRM Basics is a purpose-built engagement platform designed specifically for Medical Science Liaisons (MSLs). It empowers medical teams to foster deep, scientific relationships with Key Opinion Leaders (KOLs) by capturing rich interaction data and providing the insights needed to drive meaningful scientific exchange.

Veeva PromoMats Basics provides the essential end-to-end solution for MLR, Claims, and Digital Asset Management (DAM), guaranteeing intuitive content management and compliant approval of all your promotional content.