Pharma Compliance Consulting, Built on Integrity - Inspection-Ready.
Pharmaceutical CSV, QA, CQV, and GMP consulting services across the Middle East and beyond - honest findings, clear documentation, inspection-ready outcomes. Aligned with FDA 21 CFR Part 11, EU GMP Annex 11, and GAMP 5. Serving regulated operations in Jordan, UAE, KSA, Egypt, and globally.
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
AI-assisted validation lifecycle management. 30 document builders, one compliant platform.
→Not sure where to start?
Tell us your situation. We'll find what matters most and give you a clear path forward.
Start Free AssessmentTraining 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.
The only validation software built specifically for pharma compliance teams. AI-assisted, audit-ready, and deployed same-day - no consultants, no setup fees.
Concept Phase
URS, risk classification, CSV planning documents
Project Phase
IQ OQ PQ protocols, execution & reporting
Operation Phase
Change control, periodic reviews, CAPAs
Retirement Phase
Archival & decommission documentation
"One month of DVS Professional costs less than two hours of an external CSV consultant."
Everything Built In
AI Drafting
Generate protocol content in minutes instead of 2–3 weeks
FDA Compliance
Built-in alignment with 21 CFR Part 11 and EU GMP Annex 11
Full Traceability
Requirements auto-linked through every test phase automatically
Workflow Engine
Configurable approval workflows replacing manual handwritten cycles
Digital Documents
Over 1,500 paper pages saved per validation project
Same-Day Deployment
No implementation partner needed. Deploy today, validate tomorrow.
Tools to get inspection-ready
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
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
June 2026 Update
DVS-PQR Module Launched — AI Cuts Product Quality Review Time by 91%
PHARPRO June 2026: utility & software validation completed per GAMP 5 2nd Edition & EU GMP Annex 11, thermal mapping qualification training launched in Pakistan, DVS-PQR module released, and 12+ pharmaceutical clients served this month.
Read the full update →From first contact to audit-ready
A structured four-step engagement delivering real compliance outcomes - not just paperwork.
Discovery Call
We understand your current state, gaps, systems, and timeline before proposing anything.
Scoped Proposal
Clear scope, timeline, and deliverables - no vague retainers or open-ended engagements.
Structured Execution
Protocols, reviews, approvals, and documentation - done correctly and on time.
Inspection-Ready Output
Deliverables that are audit-defensible, complete, and immediately usable in your quality system.
Join 15+ inspection-ready clients
How regulated pharmaceutical manufacturers describe working with PHARPRO.
"PHARPRO supported us with strong technical understanding and practical execution. Their work added real clarity to our validation and compliance activities."
"Professional, responsive, and perfectly aligned with the demands of our regulated environment. PHARPRO delivered without ambiguity."
"PHARPRO helped us approach validation and quality in a more structured, inspection-focused way. Their risk-based methodology was exactly right."
Common questions
Questions clients ask before starting an engagement.
Start free - no commitment, no sales pitch
A 20-minute discovery call. We listen, identify your most important gaps, and give you an honest path forward - whether you work with us or not.
Phone / WhatsApp
+962 79 856 5807Location
Amman, Jordan - serving clients worldwide
Send us a message
⚡ Average response time: under 2 hours
Your next inspection won't wait.
Your competitors aren't waiting either.
PHARPRO accepts a limited number of new project engagements each quarter to maintain delivery quality. Q3 2026 has 2 slots remaining - once filled, next availability is Q4. The free assessment takes 20 minutes and costs you nothing. The alternative costs far more.
The Pharmaceutical Compliance Experts - Jordan & Worldwide
PHARPRO is a pharmaceutical compliance consulting firm based in Amman, Jordan, specialising in CSV, QA, CQV, thermal mapping, and GMP training for regulated manufacturers across the Middle East and globally. Aligned with FDA 21 CFR Part 11, EU GMP Annex 11, and ISPE GAMP 5 - our work is audit-defensible from day one.
We also offer PHARPRO DVS, an AI-assisted validation software platform that cuts documentation time by up to 30 working days per project - deployed same-day, no implementation partner needed.
Every service is delivered by practising consultants - not generalist trainers. Book your free compliance assessment today →