One connected validation lifecycle
DVS connects validation planning, user requirements, risk assessment, specifications, qualification protocols, test documentation, traceability and summary reporting. Teams can work from a shared lifecycle instead of manually reconciling independent files.
Connected records improve visibility of missing evidence, changes, review status and requirement coverage before project closure.
AI-assisted drafting with human control
Built-in drafting intelligence helps qualified users prepare structured first drafts from approved project inputs. Users remain responsible for technical review, correction, approval and the final validation decision.
This model uses AI to reduce repetitive preparation work while preserving accountability, data integrity and quality-system governance.
Controls for regulated teams
The platform supports role-based access, controlled workflows, audit-trail capability, electronic review and approval, lifecycle status and connected traceability. Each company must assess intended use, configure governance and validate the system for its own regulated use.
DVS is designed to support Part 11 and Annex 11 assessments; compliance depends on the complete technical and procedural environment.
From pilot to enterprise use
Organizations can begin with a representative validation project, confirm configuration and roles, validate intended use and compare cycle time and rework with the approved baseline. The pilot provides evidence for controlled scaling.
PHARPRO supports demos, implementation planning, onboarding, validation assistance and enterprise scoping.
Frequently asked questions
Is PHARPRO DVS already validated for every customer?
No supplier platform is automatically validated for every intended use. Each regulated company must assess and validate its configured use.
Does DVS include requirements traceability?
Yes. The platform is designed to connect requirements with related validation and testing records through the lifecycle.
Can we request a live demonstration?
Yes. PHARPRO provides focused demonstrations based on the systems, documents and compliance priorities your team wants to improve.
See PHARPRO DVS in action
Explore connected validation documents, requirements traceability, controlled review and AI-assisted drafting with qualified human approval.
Explore PHARPRO DVS & book a demo →