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15+ regulated companies already inspection-ready with PHARPRO

The Pharma Compliance Experts — Inspection-Ready.

PHARPRO is the Middle East's most trusted pharmaceutical validation & compliance firm. 10+ years of delivering audit-defensible outcomes across 7+ countries — we find and close compliance gaps before regulators do.

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PHARPRO DVS — Digital Validation Software
AI-Powered · FDA & EU GMP Compliant
30 working days saved per project
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10+
Years Experience
22+
Projects Completed
15+
Active Clients
7+
Countries Served
The Cost of Inaction

What happens when compliance gaps go unaddressed

Pharmaceutical companies don't get second chances with regulators. One inspection, one gap, one finding — and the consequences compound fast.

FDA Warning Letter

18 months

Average remediation time after receiving a Warning Letter — with production halted, external consultants at emergency rates, and brand credibility destroyed.

Import Alert / Market Ban

$2M+

Estimated annual revenue impact of a U.S. import alert. Market access revoked while your competitors fill the gap — often permanently.

Production Shutdown

6–24 mo.

Duration of regulatory-forced production suspensions while companies remediate findings. Every shutdown day is direct, unrecoverable revenue loss.

Don't wait for the inspection letter. Find your gaps now — before regulators do.

Get Your Free Gap Assessment → No commitment. No sales pitch. Honest assessment in 20 minutes.
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.

Unvalidated systems = automatic finding under FDA 21 CFR Part 11
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Quality Assurance & Gap Assessment

Find gaps before auditors do. SOP reviews, QA assessments, and CAPA support to close findings fast.

Undocumented gaps become CAPA backlogs that compound until inspection day
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CQV & Thermal Mapping

Equipment and utility qualification, plus temperature distribution studies for controlled storage environments.

Unqualified equipment = batch rejections, product recalls, regulatory holds
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GMP Training

CSV, data integrity, and GMP training tailored to your team's actual gaps. Delivered on-site or online.

Untrained staff = the #1 root cause cited in regulatory audit findings
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Digital Validation Software

AI-assisted validation lifecycle management. 30 document builders, one compliant platform.

Manual validation = 10× the time, 10× the error rate vs. a purpose-built platform
→

Not sure where to start?

Tell us your situation. We'll find what matters most and give you a clear path forward.

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GMP 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 sector

30 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.

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V-Model Lifecycle
Full Validation Coverage

Concept Phase

URS, risk classification, CSV planning documents

Save 60 working hours

Project Phase

IQ OQ PQ protocols, execution & reporting

Save 200 working hours

Operation Phase

Change control, periodic reviews, CAPAs

Save 132 working hours

Retirement Phase

Archival & decommission documentation

Save 136 working hours
30 working days
total savings per validation project

"One month of DVS Professional costs less than two hours of an external CSV consultant."

DVS Platform

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.

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. Free. No credit card required.

  • 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
Download Free Checklist Instant access · No spam
Free Quiz: Is Your Site Inspection-Ready? 10 yes/no questions. 2 minutes. Get your personalised compliance risk score — Low, Medium, or High — and know exactly where you stand before your next FDA or EU GMP inspection.
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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.

Client Feedback

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."

AG
Axantia Group
Quality & Validation · Jordan
Verified Client
★★★★★

"Professional, responsive, and perfectly aligned with the demands of our regulated environment. PHARPRO delivered without ambiguity."

DD
Dar Al Dawa
Quality Assurance · Jordan
Verified Client
★★★★★

"PHARPRO helped us approach validation and quality in a more structured, inspection-focused way. Their risk-based methodology was exactly right."

AH
Al Hayat Pharmaceuticals
CSV & Compliance · Jordan
Verified Client
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.
Every month of delay is a month closer to an inspection you're not ready for. Your free assessment takes 20 minutes. Book it today →
Contact

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 5807

Location

Amman, Jordan — serving clients worldwide

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⚡ Average response time: under 2 hours

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Limited Availability — Q3 2026

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.

Only 2 Q3 2026 project slots remaining
Reserve My Slot Now WhatsApp Chat
Free initial assessment No commitment required Response within 2 hours 22+ projects delivered
About PHARPRO

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 →