🎓 Upcoming GMP training sessions - dates to be announced. Register your interest →
Pharmaceutical GMP Training
#GMPTraining #PharmTraining #CSVTraining

GMP Training by Practitioners.

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.

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Online - Live interactive On-site - Your facility
Upcoming Courses

Upcoming Courses - Dates to be announced.

Live instructor-led sessions - online and on-site. Materials and a PHARPRO Certificate of Attendance included. Register your interest now to be notified when dates are confirmed.

📅 Date to be announced

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.

OnlineOn-site
📅 Date to be announced

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.

OnlineOn-site
📅 Date to be announced

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.

OnlineOn-site
📅 Date to be announced

GMP Training

Core GMP principles for pharmaceutical manufacturing - regulatory expectations, documentation, CAPA, change control, deviation management, and audit readiness. Practical and regulation-aligned.

OnlineOn-site
📅 Date to be announced

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.

OnlineOn-site
📅 Date to be announced

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.

OnlineOn-site
📅 Date to be announced

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.

OnlineOn-site
📅 Date to be announced

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.

OnlineOn-site
📅 Date to be announced

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.

OnlineOn-site
📅 Date to be announced

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).

OnlineOn-site
📅 Date to be announced

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.

OnlineOn-site
What our clients say

Trusted by pharmaceutical teams across MENA

"PHARPRO supported us with strong technical understanding and practical execution. Their work added real clarity to our validation and compliance activities."

Axantia Group
Pharmaceutical Manufacturer

"Professional, responsive, and perfectly aligned with the demands of our regulated environment. PHARPRO delivered without ambiguity."

Dar Al Dawa
Pharmaceutical Manufacturer, Jordan

"PHARPRO helped us approach validation and quality in a more structured, inspection-focused way. Their risk-based methodology was exactly right."

Al Hayat Pharmaceuticals
Pharmaceutical Manufacturer, Jordan
Reserve your seat - Upcoming sessions

Register for a course

Tell us which course you are interested in. We confirm by WhatsApp or email within one business day and send pre-reading materials before the session.

Dates to be announced - register your interest now
All upcoming courses are open for interest registration. Dates will be confirmed and communicated to registered participants first. Registering holds your place at no obligation.
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Need customised in-house delivery? Contact us to discuss →

Completed Programmes

Building expertise across the sector

These programmes have been successfully delivered. Contact us if you'd like to request a scheduled or bespoke run.

Excel Sheet Validation
CSV Training
ISO 13485
EU GMP Annex 1
Thermal Mapping Training
GMP Training
Data Integrity Training
Why PHARPRO Training

Practical. Expert-led. Regulation-aligned.

Every course is delivered by working pharmaceutical consultants - not generalist trainers. The content reflects current regulatory expectations.

Expert Instructors

Courses are led by PHARPRO consultants with active project experience - not theoretical trainers. Real cases, real 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.

FAQ

Training questions

Yes. All programmes are available online and on-site. Online sessions are live and interactive - not pre-recorded. Participants receive course materials and a certificate of attendance upon completion.
QA/QC teams, validation engineers, regulatory affairs specialists, manufacturing supervisors, and laboratory staff. No prior specialised knowledge required - courses are calibrated to the practical needs of working pharma teams.
Use the Register Interest button on any course card, or contact us at [email protected]. We will confirm your registration and send joining instructions within one business day.
Yes. Bespoke private training can be arranged for your team - delivered online or at your facility, with content tailored to your systems, SOPs, and specific compliance gaps. Contact us to discuss dates and scope.
All participants receive a PHARPRO Certificate of Attendance - a verifiable record of professional training suitable for training files, annual training records, and regulatory submissions.
All public programmes are delivered in English. Arabic-medium sessions are available for private and on-site engagements on request - providing the full programme content in Arabic for pharmaceutical teams across Jordan and the wider MENA region.
The two-day CSV training covers risk-based validation methodology, FDA 21 CFR Part 11, EU GMP Annex 11, ISPE GAMP 5 system categories, URS development, IQ/OQ/PQ protocol writing, audit trail review, and change control. Participants leave with a practical framework they can apply directly to their own validation projects.
PHARPRO GMP training prices vary by course format and delivery type. Public online courses are competitively priced per seat. Private on-site or online sessions are priced per cohort with group discounts for teams of five or more. Contact us for the current fee schedule.
All PHARPRO training programmes are eligible for self-reported CPD hours. Participants receive a PHARPRO Certificate of Attendance documenting the course title, content summary, duration, and delivery date - suitable for professional development portfolios, annual training files, and regulatory submissions.
Yes. PHARPRO Certificates of Attendance provide documented evidence of pharmaceutical GMP training suitable for training files reviewed during FDA, EU GMP, WHO, and JFDA inspections. The certificate includes instructor credentials, course content summary, delivery date, and participant confirmation - meeting typical inspector expectations for third-party training records.
PHARPRO offers three specialised GMP training courses: Computerized System Validation (CSV) - a two-day programme covering FDA 21 CFR Part 11, EU GMP Annex 11, and ISPE GAMP 5; Cleaning Validation - covering EU GMP Annex 15, acceptance criteria, and MACO calculations; and Compressed Air Testing & Qualification - covering ISO 8573 standards and qualification protocols. All courses are available online or on-site.
Yes. PHARPRO is based in Amman, Jordan, and its GMP training is specifically designed for pharmaceutical teams across the MENA region - including Jordan, UAE, Saudi Arabia, Egypt, Kuwait, and Bahrain. Courses align with FDA, EU GMP, WHO, and regional authority requirements (JFDA, SFDA, UAE MOH). Private Arabic-medium sessions are available on request.
PHARPRO's CSV training is a two-day programme covering risk-based validation methodology, FDA 21 CFR Part 11, EU GMP Annex 11, ISPE GAMP 5 categorisation, URS writing, IQ/OQ/PQ protocol development, audit trail review, and change control. Available as a public open-enrolment course or as a private in-house session tailored to your team's systems and compliance gaps.
For QA engineers, the most impactful GMP training addresses exactly what inspectors examine: computerized system validation (CSV), data integrity, CAPA, and inspection readiness. PHARPRO's practitioner-led courses cover real inspection scenarios, applicable regulatory frameworks (FDA, EU GMP, WHO), and practical techniques that apply directly to day-to-day compliance work. Contact us to discuss the right course for your team.
Yes. PHARPRO offers Arabic-medium GMP training for private and on-site engagements across Jordan and the wider MENA region. Public courses are delivered in English. Arabic-language sessions cover the full programme content - CSV, cleaning validation, or compressed air qualification - and are available for pharmaceutical teams who prefer instruction in Arabic. Contact us at [email protected] to arrange a session.
PHARPRO GMP training is led by practitioners who actively work on live pharmaceutical validation and QA projects - not academic presenters. Courses are smaller, more interactive, and directly applicable to the regulatory environments that MENA-region pharma teams operate in. Unlike large international bodies, PHARPRO can tailor content to your organisation's SOPs, systems, and inspection history - and deliver in English or Arabic.
Related Insights

Go deeper on GMP training topics

In-depth guides from the PHARPRO team on CSV, cleaning validation, 21 CFR Part 11, and compressed air - the topics our courses cover in detail.

CSV Guide
CSV for SaaS & Cloud Applications in Pharma
Validation approach, vendor qualification, and documentation strategy for cloud-hosted GxP systems.
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GAMP 5
GAMP 5 Risk Categories: How to Classify Your System
What changed in the Second Edition and how to assign the correct category to any computerized system.
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Compliance
21 CFR Part 11 Audit Trail: What Your System Must Capture
Exactly which events must be logged, how to configure compliant audit trails, and common gaps inspectors find.
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Qualification
IQ OQ PQ Explained: What Each Phase Requires
Regulatory basis, documentation requirements, and what auditors look for in each qualification phase.
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Documentation
How to Write a URS for a Pharmaceutical Computerised System
Structure, GxP requirements, and a step-by-step guide to a compliant User Requirements Specification.
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Related Services

Complete compliance support

Computerized System Validation

End-to-end CSV consulting - URS, risk classification, IQ/OQ/PQ protocols, and Validation Summary Report.

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Quality Assurance & Gap Assessment

QA gap assessments, SOP development, CAPA management, and inspection readiness reviews.

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CQV & Thermal Mapping

Equipment commissioning, IQ/OQ/PQ, and temperature mapping for controlled pharmaceutical environments.

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Now accepting Q3 2026 engagements

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Based in Amman, Jordan · Serving clients worldwide · Response within 24 hours