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PHARPRO DVS - Digital Validation Software
#ValidationSoftware #DigitalValidation #Part11Software

Stop managing validation in
Word files and spreadsheets.

30 document builders. Full RTM. Part 11 e-signatures. Same-day deployment.

PHARPRO DVS is pharmaceutical validation software built specifically for CSV teams - replacing Word and Excel with a connected, audit-ready platform. Used by pharma manufacturers across Jordan, UAE, Saudi Arabia, and Egypt for FDA 21 CFR Part 11 and EU GMP Annex 11 compliant validation programmes. From $253/month. No installation required.

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FDA 21 CFR Part 11 compliant
EU GMP Annex 11 aligned
No installation - web-based SaaS
Same-day deployment
Trusted by pharma teams in Jordan, KSA, UAE & Egypt
Free 30-minute platform walkthrough

Book a personalised DVS demo

We'll walk through the platform with your validation programme in mind - document builders, RTM, e-signatures, and deployment. No commitment required.

Teams across MENA, EU & the US use DVS
Typically respond within 2 business hours
Limited demo slots available this week
Response within 24 hours · No commitment
Prefer to message directly? Chat on WhatsApp
3 wks → 4 days
IQ/OQ/PQ cycle time
reduced by DVS teams
30
pharma-specific
document builders
60–75%
reduction in
documentation time
Same day
deployment
no installation
$253/mo
Professional plan
all features included
Platform Features

Everything a pharma validation team needs

PHARPRO DVS replaces disconnected templates with a single, regulated platform covering the entire validation lifecycle.

AI Document Drafting

AI generates first-draft validation documents in seconds - URS, risk assessments, IQ/OQ/PQ protocols, and more - aligned with current regulatory guidance.

30 Document Builders

Purpose-built templates for every stage: Validation Master Plan, URS, Risk Assessment, IQ/OQ/PQ, Test Scripts, Discrepancy Log, RTM, and VSR.

Requirements Traceability Matrix

Automated RTM links user requirements to test cases and test results - providing full traceability from URS to final report.

21 CFR Part 11 E-Signatures

Compliant electronic signatures with full audit trail. Role-based access controls, meaning, date, time, and user attribution on every signature event.

Regulatory-Quality PDF Export

Generate submission-ready PDFs with proper formatting, signatures, version history, and document control headers - inspection-ready from day one.

Workflow Engine

Configurable review and approval workflows ensure documents go through the right hands in the right order, with automated notifications and status tracking.

Document Library

30 pharma validation document builders

Every document type your validation programme needs - pre-structured, regulation-aligned, and ready for AI drafting.

Validation Master Plan (VMP)
User Requirements Spec (URS)
Functional Requirements Spec
Risk Assessment Report
GAMP 5 Category Assessment
Supplier Qualification Report
Vendor Assessment Questionnaire
Installation Qualification (IQ)
Operational Qualification (OQ)
Performance Qualification (PQ)
Test Scripts & Test Cases
Discrepancy/Deviation Report
Traceability Matrix (RTM)
Validation Summary Report (VSR)
Change Control Record
Periodic Review Report
Data Migration Validation
Decommissioning Plan
Audit Trail Review Report
21 CFR Part 11 Assessment
Annex 11 Assessment
Data Integrity Assessment
System Retirement Plan
SOPs (multiple templates)
Getting Started

Up and running in hours, not months

No IT project. No implementation consultant. No waiting for a procurement cycle.

1

Book a free 30-min demo

We walk through the platform live, tailored to your systems - document builders, RTM, e-signatures, and AI drafting. No slides. No sales pitch. Just the platform and your questions.

2

Get access - same day

No installation, no IT ticket. Your team logs in via browser. We configure your workspace, set up role-based access, and onboard your team - typically within a few hours of subscribing.

3

Generate compliant docs from day one

AI drafts your first IQ/OQ/PQ protocol. The RTM builds automatically as you work. Every signature is Part 11–compliant. Your first validation project starts the day you subscribe.

Book My Free Demo → No commitment · Response within 2 business hours
Pricing

Plans for every team size

Transparent pricing. No hidden fees. Cancel anytime. All plans include access to the full document library.

Professional

$253/month

Up to 10 concurrent users. Best for small validation teams.

  • Unlimited projects & documents
  • All 30 document builders
  • AI drafting assistant
  • Full RTM traceability
  • 21 CFR Part 11 e-signatures
  • Regulatory-quality PDF export
  • Email support
Book a Free Demo →
Most Popular

Team

$500/month

Up to 25 concurrent users. Best for mid-size quality teams.

  • Everything in Professional
  • Up to 25 concurrent users
  • Dedicated onboarding session
  • Priority support response
  • Advanced workflow configuration
  • Role-based access controls
Book a Free Demo →

Enterprise

Custom

Unlimited users. For large organisations and multi-site deployments.

  • Everything in Team
  • Unlimited concurrent users
  • Custom SLA & uptime guarantee
  • SSO & Active Directory integration
  • Dedicated implementation support
  • Custom validation package available
Book a Demo →
FAQ

Common questions about PHARPRO DVS

PHARPRO DVS (Digital Validation Software) is an AI-assisted, web-based platform that helps pharmaceutical and life sciences teams create, manage, and approve validation documentation - from URS through to Validation Summary Report - fully aligned with FDA 21 CFR Part 11 and EU GMP Annex 11.
PHARPRO DVS replaces Word templates and disconnected spreadsheets with a connected, traceable platform. AI drafting, built-in regulatory logic, and automated RTM eliminate manual errors and significantly reduce documentation time. All documents are version-controlled with a full audit trail.
Yes. PHARPRO DVS is built around FDA 21 CFR Part 11 and EU GMP Annex 11 - including electronic signatures, audit trails, access controls, and data integrity. The platform itself can be validated for use in GxP environments.
PHARPRO DVS includes 30 pharmaceutical-specific document builders covering the full validation lifecycle: Validation Master Plan, URS, Risk Assessment, IQ/OQ/PQ protocols, Test Scripts, Discrepancy Reports, Traceability Matrix, and Validation Summary Report.
PHARPRO DVS is a web-based SaaS - no installation required. Teams can be onboarded and generating compliant documentation on the same day. Request a demo via our contact form to see the platform in action.
Yes. PHARPRO DVS is designed to support its own validation. We provide a vendor qualification package - including system description, architecture overview, and security documentation - to support your IQ/OQ of the platform in line with GAMP 5 Category 4 requirements.
An RTM maps every user requirement from the URS to its corresponding test cases in the IQ/OQ/PQ protocols and then to the actual test results - providing end-to-end traceability proving every requirement has been tested and met. PHARPRO DVS generates the RTM automatically as you build and execute protocols.
Yes. DVS includes a dedicated GAMP 5 Category Assessment document builder that guides teams through classifying a system as Category 1, 3, 4, or 5 and links the classification directly to the appropriate validation depth and document set.
PHARPRO DVS pricing starts at $253/month for the Professional plan (up to 10 users), $500/month for Team (up to 25 users), and custom pricing for Enterprise. All plans include all 30 document builders, AI drafting, automated RTM, and FDA 21 CFR Part 11 compliant e-signatures. No per-document fees. Annual plans available with a discount.
Most PHARPRO DVS customers report a 60–75% reduction in documentation time per validation project. For a team running 5–10 CSV projects per year, this translates to hundreds of consultant-hours saved annually. At $253/month, DVS typically pays for itself within the first single validation project through time savings alone.
Yes. PHARPRO DVS supports cleaning validation documentation as part of its broader equipment validation workflow. The platform includes document builders for cleaning validation protocols, MACO calculation records, swab and rinse sampling plans, and analytical testing documentation - all formatted to EU GMP Annex 15 and FDA cleaning validation guidance.
Yes. PHARPRO offers a free 30-minute live demo where our team walks you through all 30 document builders, AI drafting, RTM generation, and the e-signature workflow - tailored to your team's specific validation use case. Request a demo via the form above and we will confirm within one business day.
PHARPRO DVS is purpose-built for pharmaceutical validation teams - 30 document builders covering the full CSV lifecycle, AI-assisted drafting, automated RTM, and FDA 21 CFR Part 11 compliant e-signatures. Unlike general-purpose QMS platforms, DVS is validation-native: no configuration overhead, same-day deployment, no per-document fees. Book a free demo to see it in action.
MasterControl, Veeva Vault QualityDocs, and Qualio are broad QMS platforms that require significant configuration to support CSV workflows. PHARPRO DVS ships with 30 pre-built pharmaceutical validation templates, automated RTM, and built-in Part 11/Annex 11 logic. DVS is typically running on day one with no professional services engagement - and is significantly more affordable for teams focused specifically on computerized system validation.
Yes. PHARPRO DVS replaces disconnected Excel spreadsheets and Word templates with a single connected environment where requirements, protocols, test results, and traceability are all linked - eliminating version control problems, RTM maintenance burden, and audit trail gaps. Documents export to regulatory-quality PDF format, ready for inspection or regulatory submission.
Yes. PHARPRO DVS is a web-based SaaS platform serving pharmaceutical companies across the MENA region - Jordan, UAE, Saudi Arabia, Egypt, Kuwait, and beyond. PHARPRO's team provides onboarding and support in both English and Arabic. The platform is used by manufacturers and consultants running FDA, EU GMP, and WHO-aligned validation programmes across the Middle East.
PHARPRO DVS uses AI to generate first-draft validation documents - URS sections, IQ/OQ/PQ test cases, and risk assessment entries - based on system type, regulatory framework, and GAMP 5 category. This eliminates hours of boilerplate writing per project. All AI-generated content is reviewed and approved by the validation team before execution, maintaining human oversight and full GxP traceability.
Who Uses DVS

Built for every role in the validation lifecycle

From validation planning to regulatory submission - DVS supports the whole team, not just the document author.

QA Managers

Review and approve validation documents without chasing paper. Configurable approval workflows keep every signature on track and fully auditable.

CSV & Validation Leads

Generate first-draft IQ/OQ/PQ protocols in minutes using AI. The automated RTM links every requirement to a test case - no manual cross-referencing.

Validation Engineers

Execute test scripts digitally with Part 11–compliant e-signatures. No hand-written sign-offs, no scanned PDFs - results recorded directly in the platform.

Regulatory Affairs

Export submission-ready PDFs with full version history, electronic signatures, and document control headers - inspection-ready from day one.

IT & System Owners

No installation, no infrastructure. Web-based SaaS - teams are onboarded and generating compliant documentation on the same day access is granted.

CROs & Consultancies

Manage multiple client projects in one platform. Separate workspaces, shared document libraries, and branded exports - all in a single subscription.

Why DVS

PHARPRO DVS vs Word/Excel/Paper

Most teams spend 60–80% of validation time on documentation. DVS changes that ratio.

Feature PHARPRO DVS Word / Excel / Paper
IQ/OQ/PQ first draft Minutes (AI-assisted) Days to weeks
Requirements Traceability Matrix Automated & live Manual, error-prone
FDA 21 CFR Part 11 e-signatures Built-in & compliant Not supported
Audit trail Automatic & tamper-proof Manual or absent
Inspection-ready PDF export One click Hours of reformatting
Time to deploy Same day Weeks of template setup
See It Live

Your team could cut IQ/OQ/PQ cycle time from weeks to days.

Book a 30-minute walkthrough tailored to your systems - no slides, no pitch deck. Just the platform and your questions.

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Customer Reviews

What validation teams say about DVS

"DVS cut our IQ/OQ/PQ documentation cycle from three weeks to under four days. The AI drafting handles the boilerplate instantly and the built-in RTM means we stop chasing traceability spreadsheets. Our last FDA inspection came back with zero data-integrity observations."

RA
Reem A.
Validation Manager

"We evaluated three platforms before choosing DVS. The 21 CFR Part 11 compliance is genuine - the e-signature workflow and audit trail are exactly what the regulation demands, not a workaround. Our QA team was generating production-quality protocols within a day of onboarding."

KM
Khalid M.
QA Director

"As a consultant managing validation for five clients simultaneously, DVS is the only platform that gives me separate workspaces with shared document libraries. The 30 document builders cover every deliverable from URS to VSR. I recommend it to every site still running validation on Word templates."

NT
Nour T.
CSV Consultant
Related Insights

Go deeper on pharmaceutical validation

In-depth guides from the PHARPRO team on validation software, FDA compliance, and documentation best practice.

Buyer's Guide
Pharma Validation Software: Buyer's Guide 2026
How DVS and competing platforms compare - what to look for before you buy.
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Deep Dive
AI Validation Lifecycle Software for Pharma
How AI is changing IQ/OQ/PQ documentation - and what it still can't replace.
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CSV Guide
CSV for SaaS & Cloud Applications in Pharma
Validation approach, vendor qualification, and documentation for cloud-hosted systems.
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Compliance
21 CFR Part 11 Audit Trail: What Your System Must Capture
Exactly which events must be logged, how to configure compliant audit trails, and common gaps.
→
Compliance
FDA 21 CFR Part 11: Data Integrity Requirements
Electronic records, e-signatures, and audit-trail requirements every regulated system must meet.
→

Ready to modernise your validation programme?

Book a free 30-minute demo - we'll walk through DVS with your specific systems and documents in mind.

Book My Free Demo → Ask on WhatsApp