Computerized System Validation
Risk-based CSV strategy, URS, validation planning, IQ/OQ/PQ, requirements traceability, audit-trail review and validation closure aligned with GAMP 5, EU GMP Annex 11 and FDA 21 CFR Part 11.
About PHARPRO
Pharmaceutical compliance expertise built around accountable delivery.
PHARPRO is a founder-led consultancy helping regulated pharmaceutical and life-sciences organisations turn requirements into practical documentation, qualified systems, defensible evidence and capable internal teams.
12 completed engagements2 active projects · August 20267 PHARPRO marketsEnglish and Arabic
Company profile
A specialist, founder-led partner for complex compliance work
PHARPRO Consultation Company L.L.C FZ was established in the UAE in 2023. Technical delivery is led by founder Mohammad Awawdeh from Amman, Jordan. PHARPRO engagements have reached Jordan, the UAE, Switzerland, Iraq, Egypt, Pakistan and Syria. Mohammad’s earlier Saudi Arabia site-establishment work was completed during his employment with MS Pharma and is presented separately from PHARPRO’s company record.
Quality Assurance and Inspection Readiness
GMP gap assessments, data-integrity reviews, CAPA, SOP systems, mock audits and remediation plans designed around the applicable authority, product and operating model.
CQV and Thermal Mapping
Qualification of equipment, HVAC, utilities, warehouses and cold rooms, including DQ/IQ/OQ/PQ, risk-based protocols and clear acceptance evidence.
Training and Digital Validation
Practical GMP and CSV training in English or Arabic, plus PHARPRO DVS for controlled, AI-assisted validation document workflows with human review and approval.
Verified business record
As of August 2026: 12 completed consulting and training engagements, two active projects, seven PHARPRO markets and six or more organisations trained.
Transparent client evidence
Named project scopes are separated from confidential outcomes. Logos, participant photographs, quotations and performance metrics are published only with confirmation of reuse rights.
How we work
Evidence first. Clear scope. No compliance theatre.
PHARPRO’s role is to identify risk, build usable controls and make the resulting evidence easy to defend. Regulatory claims are always evaluated against the client’s actual product, process, system and target market.
1. Define the decision
Agree the regulatory scope, intended use, responsibilities, acceptance criteria and final decision owner before creating documents.
2. Follow the risk
Prioritise patient safety, product quality and data integrity so effort is concentrated where failure has the greatest impact.
3. Leave a usable system
Deliver controlled documents, traceable evidence and knowledge transfer that the client’s own quality team can maintain after project closure.
Leadership
Founder-led, practitioner-led
PHARPRO was founded by Mohammad Awawdeh, a pharmaceutical compliance consultant with more than seven years of hands-on validation experience. He leads sales conversations, project scoping and technical delivery across CSV, quality assurance, CQV, GMP training and digital validation—so the person defining the work remains accountable for its execution.
Start with the compliance decision you need to make.
Share the system, inspection priority or validation challenge. PHARPRO will recommend a practical starting point and normally respond within one business day.
Request a free assessment