Pharmaceutical Compliance Consulting in Jordan
PHARPRO is headquartered in Amman and delivers CSV validation, QA gap assessments, CQV, thermal mapping, and GMP training for pharmaceutical companies across Jordan - on-site and remotely. Fully aligned with Jordan Food and Drug Administration (JFDA) requirements.
Understanding the Jordan Pharmaceutical Landscape
Jordan has one of the most mature and export-driven pharmaceutical industries in the Arab world, with over 30 licensed manufacturers exporting to more than 60 countries. The Jordan Food and Drug Administration (JFDA) regulates manufacturing, import, and distribution of medicinal products, increasingly aligning its GMP inspection regime with PIC/S and WHO standards. Export-focused manufacturers - particularly those supplying regulated markets in the US, EU, and Gulf - face layered regulatory expectations from both the JFDA and international authorities.
PHARPRO is based in Amman. That means Jordan clients get the fastest mobilisation, lowest overhead, and consultants who understand the local regulatory environment directly - not from a distance.
Compliance Services for Jordan Pharma
On-site and remote support - delivered at the pace your programme requires. Faster mobilisation than any non-Jordanian provider.
CSV Validation
Full-lifecycle CSV for pharma software and laboratory systems. IQ/OQ/PQ, URS, risk classification, and audit trail review - aligned with EU GMP Annex 11, FDA 21 CFR Part 11, and JFDA computerised system expectations.
QA & Gap Assessment
Gap assessments against JFDA GMP guidelines and international standards. SOP reviews, CAPA management, data integrity programmes, and quality system audits.
CQV & Thermal Mapping
Equipment and utility qualification (IQ/OQ/PQ) and temperature mapping studies for pharmaceutical warehouses, cold chain facilities, and manufacturing areas across Jordan.
GMP Training
Customised GMP training for Jordan pharma teams - data integrity, CSV fundamentals, IQ/OQ/PQ methodology, and JFDA inspection readiness. Available in English and Arabic.
Inspection Readiness
Mock audits, system walkthroughs, and documentation reviews to prepare your Jordan site for JFDA GMP inspections and international authority audits.
CAPA Management
Root cause analysis, corrective and preventive action planning, and CAPA effectiveness checks - aligned with ICH Q10 and JFDA quality system requirements.
Regulations We Work Within in Jordan
All PHARPRO work in Jordan is aligned with applicable local and international regulatory standards.
Frequently Asked Questions - Jordan
Yes. PHARPRO is headquartered in Amman and serves pharmaceutical manufacturers, distributors, and contract organisations across Jordan - both on-site and remotely. We have supported Jordan clients with CSV validation, QA gap assessments, GMP training, thermal mapping, and JFDA inspection readiness.
Pharmaceutical companies in Jordan must comply with Jordan Food and Drug Administration (JFDA) requirements, including JFDA GMP Guidelines, WHO GMP Guidelines (TRS 986), and PIC/S GMP Guidelines. Export-focused manufacturers must additionally align with the regulatory requirements of their target markets - including EU GMP, FDA 21 CFR, and Gulf SFDA/MoHAP standards.
Yes. Because PHARPRO is based in Amman, on-site work in Jordan - including thermal mapping, facility walkthroughs, mock JFDA inspections, and hands-on training - can be arranged quickly with no international travel overhead. Remote delivery is equally available for documentation, CSV, and QA work.
Faster than any other market. PHARPRO is based in Amman, so remote work can begin within 1–3 business days for urgent situations. On-site engagements typically begin within a week of proposal agreement. Contact us for a free initial compliance assessment.
Ready to start your Jordan compliance project?
Start with a free 30-minute compliance assessment. No commitment, no sales pitch. We're based in Amman - we can meet in person.