GMP & CSV Pharmaceutical Training — Certified, Instructor-Led, MENA
Instructor-led CSV, Cleaning Validation, and GMP training. Online and on-site for pharmaceutical teams.
PHARPRO GMP training is delivered by practitioners who work on live pharmaceutical validation and QA projects across the MENA region. Courses cover FDA 21 CFR Part 11, EU GMP Annex 11, and WHO requirements - applicable to pharmaceutical companies in Jordan, UAE, Saudi Arabia, and Egypt. Available online and on-site, in English or Arabic.
Upcoming Courses — October 2026
GMP training runs 7–8 October and CSV training runs 27–28 October. Both are live, instructor-led and available online or in Amman.
Computerized System Validation (CSV)
Hands-on CSV methodology training covering risk-based approaches, FDA 21 CFR Part 11, EU GMP Annex 11, ISPE GAMP 5, URS development, IQ/OQ/PQ protocol writing, and audit trail review exercises.
Compressed Air Testing & Qualification
Specialist training on compressed air testing and qualification in pharmaceutical manufacturing - ISO 8573, risk assessment, sampling procedures, analytical testing, acceptance criteria, and GMP compliance documentation.
Cleaning Validation
Principles, regulatory requirements, and practical implementation of cleaning validation for pharmaceutical manufacturing. Covers EU GMP Annex 15, FDA guidance, sampling strategies, acceptance criteria (MACO), and documentation.
GMP Training
Core GMP principles for pharmaceutical manufacturing - regulatory expectations, documentation, CAPA, change control, deviation management, and audit readiness. Practical and regulation-aligned.
Thermal Mapping Training
Temperature distribution studies and thermal mapping qualification for warehouses, cold rooms, and manufacturing areas. Covers sensor placement, protocols, acceptance criteria, and alignment with WHO, EU GMP, and ASHRAE standards.
Good Supply & Distribution Practice (GSDP)
GDP/GSDP regulations for pharmaceutical distribution - WHO GDP guidelines, EU GDP Directive, storage and transport conditions, cold chain management, distributor qualification, and documentation requirements.
Quality Culture Training
Building a pharmaceutical quality culture - human error prevention, behavioural GMP, quality mindset, leadership in compliance, right-first-time principles, and practical culture improvement tools.
Data Integrity Training
ALCOA+ principles, FDA and MHRA data integrity expectations, audit trail review, computerised system controls, data governance frameworks, and common data integrity failure modes and remediation strategies.
Medical Devices - ISO 13485
ISO 13485:2016 quality management system requirements for medical device manufacturers - risk management (ISO 14971), design controls, traceability, post-market surveillance, and regulatory submissions.
EU GMP Annex 1 Training
The 2022 revised EU GMP Annex 1 for sterile medicinal products - Contamination Control Strategy (CCS), cleanroom design and classification, environmental monitoring programmes, and barrier technologies (RABS/isolators).
Environmental Monitoring - ISO 14644
Cleanroom classification and environmental monitoring programmes per ISO 14644 - particle counting methodology, microbial monitoring, EM trending and alert/action limits, and regulatory expectations for aseptic processing areas.
Publicly documented training delivery
The project record documents PHARADA and Al Massat Data Integrity training, JEA CSV awareness, multi-company CSV training, JPM, Tafaseel Engineering and Morgan Chemicals. Public event links are provided where available; quotations and photographs remain subject to reuse permission.
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Building expertise across the sector
These programmes have been successfully delivered. Contact us if you'd like to request a scheduled or bespoke run.
Practical. Expert-led. Regulation-aligned.
Every course is led by PHARPRO founder Mohammad Awawdeh, a working pharmaceutical validation consultant. The content reflects current regulatory expectations.
Expert Instructors
Courses are led by PHARPRO founder Mohammad Awawdeh using current project experience, practical cases and documented decisions.
Online & On-site
Live interactive sessions - not pre-recorded. Online or at your facility. Same content, same instructor, same certificate.
Course Materials
Every participant receives a full digital course pack - slides, reference templates, and worked examples - for post-course use.
Certificate of Attendance
All participants receive a PHARPRO Certificate of Attendance - a verifiable record suitable for training files and regulatory submissions.
Training questions
Go deeper on GMP training topics
In-depth guides from Mohammad Awawdeh on CSV, cleaning validation, 21 CFR Part 11, and compressed air - the topics our courses cover in detail.
Complete compliance support
Why PHARPRO
Practical GMP and CSV training support with audit-defensible outputs
PHARPRO aligns each engagement with the regulations and guidance applicable to the client’s product, market and quality system. Final responsibility and approval remain with the regulated company.