Validation teams across pharmaceutical manufacturing spend an average of 14–20 hours per system building IQ/OQ/PQ documentation from scratch. That's 14–20 hours of templates, version control, approval chasing, and last-minute reformatting before every inspection — for each system in your validated environment.
PHARPRO DVS was built to change that. In a single live session, we'll show you how our AI-assisted platform generates a complete IQ/OQ/PQ package — URS, risk assessment, RTM, qualification protocols, and reports — for your specific system type, in under 10 minutes.
No generic slides, no scripted pitch. Every demo is live, using your system type and regulatory context. Book a slot below and come with your hardest validation question.
What PHARPRO DVS Does — The Core Capabilities
AI-Assisted Document Generation
Generate URS, IQ, OQ, PQ protocols and reports with system-specific content. No blank templates. No copy-paste errors.
Automated RTM
Requirements Traceability Matrix builds automatically as you work. Every requirement links to a test, every test to a result.
21 CFR Part 11 E-Signatures
Role-based electronic signatures with meaning, intent logging, and tamper-evident audit trail. Fully Annex 11 aligned.
Risk Assessment Engine
GAMP 5 risk categorisation with heat maps, impact/probability scoring, and residual risk tracking — all built in.
30+ Document Builders
From Validation Master Plan to System Retirement Report. Every document type the CSV lifecycle requires, in one place.
Same-Day Deployment
Cloud-based, no infrastructure setup. Full validation documentation for DVS itself is provided. Onboarding in under one hour.
What Happens in Your 30-Minute Demo
DVS vs. Manual Validation: The Honest Comparison
| Capability | PHARPRO DVS | Manual / Word + Excel |
|---|---|---|
| Time to first protocol draft | Under 10 minutes | 3–8 hours |
| Automated RTM | ✓ Auto-generated | ✗ Manual, error-prone |
| 21 CFR Part 11 e-signatures | ✓ Built-in | ✗ Not available |
| Audit trail | ✓ Tamper-evident | ✗ No native trail |
| Version control | ✓ Automatic | ✗ Manual file naming |
| GAMP 5 risk assessment | ✓ Integrated | ✗ Separate spreadsheet |
| Inspection-ready export | ✓ One-click PDF | ✗ Manual compilation |
| System validation documentation | ✓ Provided by PHARPRO | ✗ You validate the tool |
Who Books a DVS Demo
Ready to see DVS live? Pick any available slot — the calendar below shows real-time availability. Sessions fill up fast around inspection season.
See Available Slots →احجز عرضاً تجريبياً لبرنامج DVS — بالعربية
برنامج PHARPRO DVS هو نظام إدارة وثائق التحقق بمساعدة الذكاء الاصطناعي — يُنشئ بروتوكولات IQ/OQ/PQ، ووثائق URS، وجداول RTM التلقائية، وتوقيعات إلكترونية متوافقة مع FDA 21 CFR Part 11 وAnnex 11 الأوروبي. احجز جلسة عرض مجانية مدتها 30 دقيقة — نُريك النظام مباشرةً حسب أنظمتك وسياقك. احجز موعدك الآن →
Common Questions About the Demo
Is the demo really free?
Yes — completely free, no credit card required. The demo is a live walkthrough of DVS tailored to your system types and validation context. There is no obligation to purchase at any stage.
What should I prepare before the demo?
Ideally, bring a list of 2–3 GxP systems you currently validate (e.g., LIMS, ERP, SCADA). The more context you share, the more specific and useful the demo becomes.
Can I include colleagues in the session?
Yes. We encourage team bookings — validation engineers, QA managers, and IT leads all benefit from seeing DVS at the same time. Simply mention the number of attendees when you book.
What are the pricing plans?
DVS plans start at $253/month (Professional — up to 10 users) and $500/month (Team — up to 25 users). Enterprise pricing is available for larger organisations. Full pricing details are shared during the demo. See full DVS overview →
Book Your Free 30-Minute DVS Demo
Choose a slot from the calendar below. You will receive a confirmation with a video link immediately after booking.
Prefer to connect directly? WhatsApp us: +962 79 856 5807 or email [email protected]