Validation Compliance Diagnostic
Focused review of systems, documents and compliance risk.
- Risk-ranked gap report
- Priority remediation roadmap
- Leadership readout
Founder-led pharmaceutical compliance
Validation transformation—from strategy to approved evidence.
PHARPRO combines founder-led consulting, turnkey validation execution and PHARPRO DVS to help regulated teams move from compliance gaps to controlled, inspection-ready outcomes.
No commitment required
Free 10-minute fit check
Response within one business day
7+
Years in Pharmaceutical Validation
12
Completed Engagements
2
Active Projects · Aug 2026
7
PHARPRO Markets Reached
Founder-led PHARPRO
Talk to the practitioner responsible for the work
PHARPRO is led by Mohammad Awawdeh, a pharmaceutical compliance consultant based in Amman and serving regulated teams across MENA and beyond. He leads client scoping and technical delivery across CSV, QA, CQV, thermal mapping, GMP training and digital validation.
PHARPRO DVS connects validation documents, requirements traceability, controlled review and approvals, with built-in drafting intelligence that remains subject to qualified human review.
Start with a direct, practical conversation—no generic pitch. Meet Mohammad, email PHARPRO or connect on LinkedIn.
Clear ways to work with PHARPRO
Start with the outcome you need.
Each engagement has a defined scope, timeline and decision-ready deliverable. Start small, execute the priority work, then scale through PHARPRO DVS where it fits.
1 Diagnose→2 Implement→3 Digitize & sustain
Inspection Readiness Sprint
Evidence-focused preparation for an upcoming inspection or customer audit.
- Critical evidence review
- Mock inspection findings
- Action and ownership plan
Turnkey Validation Delivery
One coordinated path from validation strategy through approved handover.
- VMP, URS and risk assessments
- CQV, CSV and protocol execution
- Deviation closure and reports
CQV & Thermal Mapping Package
Protocol, controlled execution, data assessment and inspection-ready reporting.
- Risk-based study design
- Calibrated execution evidence
- Final report and recommendations
PHARPRO DVS Controlled Pilot
Test one representative validation lifecycle against your approved baseline.
- Configured pilot workflow
- Onboarding and validation support
- Measured fit, effort and next-step decision
Services
Everything your compliance programme needs
Computerized System Validation
Full CSV lifecycle - planning through closure - aligned with FDA 21 CFR Part 11, EU GMP Annex 11, and GAMP 5.
→Quality Assurance & Gap Assessment
Find gaps before auditors do. SOP reviews, QA assessments, and CAPA support to close findings fast.
→CQV & Thermal Mapping
Equipment and utility qualification, plus temperature distribution studies for controlled storage environments.
→GMP Training
CSV, data integrity, and GMP training tailored to your team's actual gaps. Delivered on-site or online.
→Digital Validation Software
Connected validation lifecycle management. 30 document builders, built-in drafting intelligence and human review.
→Not sure where to start?
Tell us your situation. We'll find what matters most and give you a clear path forward.
Start Free AssessmentGMP Training
Training Programmes
Instructor-led training - on-site and online - for pharma teams. Seats are limited; register early.
Upcoming Trainings
Completed Programmes
Building expertise across the pharmaceutical sector30 Document Builders.
One Platform.
A new generation of validation workflow for pharmaceutical teams, with built-in drafting intelligence, requirements traceability and controlled review.
V-Model Lifecycle
Full Validation Coverage
Concept Phase
URS, risk classification, CSV planning documents
Reduce manual planning work
Project Phase
IQ OQ PQ protocols, execution & reporting
Reduce document rework
Operation Phase
Change control, periodic reviews, CAPAs
Simplify periodic review
Retirement Phase
Archival & decommission documentation
Keep closure evidence connected
Your baseline
measure time saved in a representative pilot
Model value using your own project volume, review effort, rework and hourly cost. Validate projections against pilot results.
DVS Platform
Everything Built In
Built-in Drafting Intelligence
Create structured first drafts faster while qualified users retain review responsibility
Compliance-supporting Controls
Controls designed to support Part 11 and Annex 11 assessments for intended use
Full Traceability
Requirements auto-linked through every test phase automatically
Workflow Engine
Configurable approval workflows replacing manual handwritten cycles
Digital Documents
Connected digital records reduce reliance on paper and disconnected files
Web-Based Deployment
No local installation; onboarding and validation effort depend on intended use.
Free Resources
Tools to get inspection-ready
Free Download
The 50-Question Pharma Compliance Checklist
Answer these 50 questions before your next FDA, EU GMP, or national authority inspection. Identify every gap your auditor will look for - and fix them first.
- Covers CSV, QA, data integrity, training & CAPA
- Aligned with FDA 21 CFR Part 11 & EU GMP Annex 11
- Print-ready - use it with your QA team today
Free Assessment
Is Your Site Inspection-Ready?
10 yes/no questions. 2 minutes. Get a personalised compliance risk score - Low, Medium, or High - and know exactly where you stand before your next inspection.
- Covers 10 critical GMP compliance areas
- Based on real FDA & EU GMP inspection findings
- Instant result - no sign-up required
Latest from PHARPRO
June 2026 Update
New
DVS-PQR Module Launched for Controlled Product Quality Reviews
PHARPRO June 2026: a utility and software validation engagement was completed, thermal mapping qualification training launched in Pakistan, and the DVS-PQR module was released.
Read the full update →How We Work
From first contact to audit-ready
A structured four-step engagement delivering real compliance outcomes - not just paperwork.
1
Discovery Call
We understand your current state, gaps, systems, and timeline before proposing anything.
2
Scoped Proposal
Clear scope, timeline, and deliverables - no vague retainers or open-ended engagements.
3
Structured Execution
Protocols, reviews, approvals, and documentation - done correctly and on time.
4
Inspection-Ready Output
Deliverables that are audit-defensible, complete, and immediately usable in your quality system.
Verified delivery record
Founder-led work across validation, quality systems, facilities and training
The dated record covers 12 completed engagements and two active projects as of August 2026. It distinguishes PHARPRO engagements from Mohammad Awawdeh’s earlier employment experience and avoids unsupported outcome claims.
CSV programmesSOP systems, software and instrument gap assessments, ERP validation, IQ/OQ/PQ and traceability.
Facility and CQV workBMS validation, conceptual pharmaceutical facility design, tender management and qualification systems.
Training deliveryCSV, data integrity and thermal mapping programmes delivered to professional bodies and pharmaceutical organisations.
Client evidence by permissionLogos, quotations and participant photographs are published only after confirmation of reuse rights.
Review the dated project track record or request a reference for an appropriate project type. References remain subject to client consent and confidentiality.
Why teams choose PHARPRO
A founder-led alternative to legacy regional consultancies
The Middle East has established GMP consultancies with decades of history. Most offer paper-based advisory work only. PHARPRO is built differently.
Consulting and software togetherPHARPRO DVS pairs validation consulting with AI-assisted validation software under qualified human review - most regional GMP consultancies offer advisory work only, with no digital platform of their own.
Evidence-first, not claims-firstEvery case study states its evidence boundary - "Pass" means project completion, not certification. Client names, logos and quotations are published only with confirmed permission.
Direct access to the practitionerYou scope and work with the consultant actually delivering the project, not an account layer routed to a delivery team.
Genuinely bilingual by designEvery service, resource and case study exists as a full Arabic build - not a translated landing page bolted onto an English-only site.
PHARPRO is younger than many regional firms, and says so plainly - the dated project record shows exactly what has been delivered so far. Compare it against your shortlist directly.
FAQ
Common questions
Questions clients ask before starting an engagement.
Manufacturers, distributors, and contract organizations - from growing regional companies to multinational operations. Particularly suited to companies preparing for regulatory inspections or implementing new systems.
Both. Remote assessments, documentation reviews, and training with no loss in quality. For hands-on work - thermal mapping, equipment qualification, on-floor audits - we travel to your site. Most engagements combine both.
A focused gap assessment: 2–3 weeks. A full CSV project: typically 6–12 weeks. We define the timeline clearly in our proposal before any commitment is made.
A discovery call to understand your current compliance situation - systems, processes, timelines, and regulatory priorities. We identify the most important areas and suggest a practical starting point. No obligation, no cost.
FDA 21 CFR Part 11, EU GMP Annex 11, ISPE GAMP 5, ICH Q10, and general GMP requirements for pharmaceutical manufacturing and distribution.
More than most companies expect. A single FDA Warning Letter triggers an average 18-month remediation process - with production halted, emergency consultant fees, and brand reputation in question. Import alerts can cost $2M+ in annual revenue. Regulatory-forced shutdowns run 6 to 24 months. In every case, reactive compliance costs 5–10× more than proactive compliance. The companies that work with PHARPRO before an inspection avoid this entirely. The ones who wait often wish they hadn't.
If a gap is already known, a short fit check can clarify the next decision. The first conversation takes 10 minutes. Request it →
Contact
Start free - no commitment, no sales pitch
A free 10-minute fit check. We listen, identify the next practical decision and tell you honestly whether PHARPRO can help.
Phone / WhatsApp
+962 79 856 5807Location
Amman, Jordan - serving clients worldwide
Send us a message
We respond within one business day.
Free Compliance Assessment
Turn compliance questions into
a clear action plan.
Share your current systems, inspection priorities, or validation challenge. PHARPRO will identify the highest-risk areas and recommend a practical starting point.
Responses normally provided within one business day
Free initial assessment
No commitment required
Response within one business day
12 completed engagements · verified August 2026