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GMP Training · Upcoming Event

GMP Training — 1 & 2 July 2026: Get Inspection-Ready in 2 Days

4 min read By Mohammad Awawdeh, PHARPRO
1 & 2 July 2026  ·  16 training hours  ·  Online & In-Person  ·  Certificate of Completion
📅
Dates
1 & 2 July 2026
Duration
16 Training Hours
📋
Modules
12 Key Modules
💻
Mode
Online & In-Person
🏅
Certificate
Upon Completion
👥
Seats
Limited

GMP is not optional — it is the regulatory backbone of every pharmaceutical operation. Inadequate training is the #1 root cause cited across FDA, EU GMP, WHO, JFDA, and SFDA inspection observations. If your team can't explain why a procedure exists, you're already at risk.

PHARPRO's GMP Training on 1 & 2 July 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 cohort is limited to 30 participants. Registration closes when full — no exceptions. Reserve your seat now →

PHARPRO GMP Training — 1 & 2 July 2026 — 12 modules, 16 training hours, Online & In-Person, Certificate of Completion

What Happens If Your Team Skips GMP Training

The real cost of undertrained pharmaceutical teams
⚠️ FDA Warning Letter triggers 18+ months of remediation
⚠️ Import alerts cost $2M+ in annual revenue losses
⚠️ One data integrity gap can pause all product releases
⚠️ Reactive compliance costs 5–10× more than proactive

Two days of training is not a cost. It's insurance — at a fraction of the price of a single inspection finding.

12 GMP Modules. Zero Gaps.

01 Regulatory Framework — WHO, EU, USFDA, SFDA
02 Pharmaceutical Quality System & Risk Management
03 GMP Documentation & Data Integrity (ALCOA+)
04 Personnel — Roles, Responsibilities & Training Records
05 Premises — Facility Design & Environmental Controls
06 Equipment Qualification (IQ, OQ, PQ)
07 OSD Process Flow & In-Process Controls
08 QC Laboratory — Testing, Sampling & Release
09 Validation Lifecycle & Quality Control
10 Deviation Management — Investigation & Documentation
11 CAPA & Change Control Systems
12 GMP Inspection Readiness & Real Case Studies

Bilingual delivery: All modules are delivered in English and Arabic. Digital training materials included for both languages.

8 days left. Seats are almost gone. Don't wait until the cohort closes — you'll miss the July intake entirely.

Secure My Seat →

This Training Is For You If…

🔬QA Officers & Managers
🏭Production & Manufacturing Staff
🌡️Warehouse & Cold Chain Managers
🧪QC Analysts & Lab Staff
⚙️Validation Engineers
📋Regulatory Affairs Professionals
🎓Pharma Graduates & New Entrants

No prior experience required. This training is built for both experienced practitioners and those new to GMP environments.

Why PHARPRO — Not a Generic Online Course

  • Practitioner-led — instructors who've written protocols, managed CAPAs, and sat in inspection rooms
  • Real case studies — FDA Warning Letter responses, deviation investigations, and actual audit observations
  • Inspector's lens — every module taught from the perspective of what regulators actually look for
  • Certificate of Completion — 16 CPD hours, suitable for your GMP training records file
  • Interactive Q&A — bring your specific challenges and get expert answers live

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.

نبذة عن التدريب — بالعربية

تدريب GMP من PHARPRO — يومان، 12 وحدة، 16 ساعة تدريبية. يُقدَّم بالعربية والإنجليزية، أونلاين ووجاهياً في عمّان. شهادة إتمام معتمدة لجميع المشاركين. المقاعد محدودة. للتسجيل: www.pharpro.co/register/gmp-training-july-2026 أو واتساب: +962 79 856 5807

Quick Answers

How do I register?

Visit the registration page, email [email protected], or WhatsApp +962 79 856 5807. State your name, company, and preferred mode (online or in-person).

Group bookings?

Yes — group registrations are welcome. Corporate in-house delivery can also be arranged for your full team. Contact us to discuss.

What do I need for online attendance?

A stable internet connection and a device with camera and microphone. Login details are sent after registration. No software installation required.

Does the certificate count toward our GMP training records?

Yes. The Certificate of Completion documents 16 hours of GMP training by PHARPRO Consultation Company — suitable for inclusion in your training records and as evidence during regulatory inspections.

GMP Training Good Manufacturing Practice Pharmaceutical Training July 2026 MENA Region Data Integrity CAPA GMP Inspection FDA EU GMP

8 Days Left. Don't Miss This Cohort.

GMP Training — 1 & 2 July 2026  ·  16 hours  ·  12 modules  ·  Certificate  ·  Online & In-Person

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