GMP is not optional — it is the regulatory backbone of every pharmaceutical operation. Inadequate training remains the #1 root cause cited across FDA, EU GMP, WHO, JFDA, and SFDA inspection observations year after year. If your team cannot explain why a procedure exists, your organisation is already at risk before an auditor walks through the door.
PHARPRO's GMP Training on 2 & 3 September 2026 gives your team 16 structured hours across 12 key modules — practical, inspection-focused, and delivered by consultants who have been in the room when auditors ask the hard questions. This is the last GMP training cohort before Q4 2026 inspection season.
This cohort is limited to 30 participants. Registration closes when full — no exceptions. Reserve your seat via WhatsApp now →
What Happens If Your Team Skips GMP Training
Two days of training is not a cost. It is insurance — at a fraction of the price of a single critical inspection observation. The September cohort is specifically timed before the Q4 regulatory inspection season peaks across the MENA region.
12 GMP Modules. Zero Gaps.
Every module is structured from the inspector's perspective — what regulators look for, what gets cited, and how to evidence compliance in your documentation system.
Bilingual delivery: All 12 modules are delivered in English and Arabic. Digital training materials provided in both languages. Certificate of Completion issued upon completion of both days.
45 days left. Seats are going. Don't wait until the cohort closes — September is the last GMP intake before Q4 inspection season.
Secure My Seat →This Training Is For You If…
No prior experience required. This training is structured for both experienced practitioners and those new to GMP environments. Participants from Jordan, UAE, KSA, Egypt, and international locations attend both online and in-person.
Why PHARPRO — Not a Generic Online Course
- Practitioner-led — instructors who have written protocols, managed CAPAs, and sat in inspection rooms across the MENA region
- Real case studies — FDA Warning Letter responses, deviation investigations, and actual audit observations from live client engagements
- Inspector's lens — every module is taught from the perspective of what regulators actually look for and how they document findings
- Certificate of Completion — 16 CPD hours, suitable for your GMP training records file as regulatory evidence
- Interactive Q&A — bring your specific site challenges and get expert, practical answers live during the session
- Group & corporate options — in-house delivery available for teams who prefer private sessions at their facility
PHARPRO has delivered pharmaceutical compliance consulting and training since 2014 — across Jordan, UAE, KSA, Egypt, and internationally. Our training is built on the same frameworks we apply in real client engagements, not adapted from generic course materials.
Why September — Before Q4 Inspection Season
Regulatory inspection activity in the MENA region peaks in Q4. Inspectors from JFDA, SFDA, UAE Ministry of Health, and international bodies (WHO prequalification, EU GMP) typically schedule facility inspections from October through December. The September cohort is deliberately timed so your team completes training and receives their certificates with full documentation in place before that window opens.
Participants who attended PHARPRO's July 2026 cohort consistently report that they identified at least one gap in their existing training records during the programme — gaps that would have been visible to inspectors. September is your last opportunity to close those gaps before Q4.
نبذة عن التدريب — بالعربية
تدريب GMP من PHARPRO — يومان، 12 وحدة، 16 ساعة تدريبية مكثفة. يُقدَّم بالعربية والإنجليزية، أونلاين ووجاهياً في عمّان. شهادة إتمام معتمدة لجميع المشاركين. الدورة في 2 و3 سبتمبر 2026 — آخر دورة GMP قبل موسم تفتيش الربع الرابع. المقاعد محدودة بـ30 مشاركاً فقط. للتسجيل عبر واتساب: +962 79 856 5807 أو بريد إلكتروني: [email protected]
Quick Answers
How do I register for the September 2026 GMP training?
WhatsApp +962 79 856 5807, email [email protected], or fill in the contact form. State your name, company, and preferred mode (online or in-person). Seats are limited to 30 — early registration is strongly advised.
Group bookings & corporate in-house delivery?
Yes — group registrations are welcome and receive priority allocation. PHARPRO also delivers the full GMP programme as a private in-house session for teams who prefer training at their own facility. Corporate packages include customised case studies drawn from your industry or product type. Contact us to discuss.
What do I need for online attendance?
A stable internet connection and a device with camera and microphone. Login credentials are sent after registration is confirmed. No software installation required — sessions run via Zoom. Materials are shared digitally before Day 1.
Does the certificate count toward our GMP training records?
Yes. The PHARPRO Certificate of Completion documents 16 hours of Good Manufacturing Practice training — suitable for inclusion in your training records file and as evidence during FDA, EU GMP, WHO, JFDA, or SFDA regulatory inspections.
Is this training recognised for continuing professional development (CPD)?
Yes. The 16 hours of structured GMP training are recognised as CPD/CPE hours and can be included in your professional development records. The Certificate of Completion specifies the training topics, duration, and delivery format.