GarnetGlobal Training Center العربية

Pharmaceutical & Laboratory

Pharmaceutical Quality Assurance

ضمان الجودة الدوائية

Download brochure (PDF) البروشور بالعربية PDF

Code
GGT-PH-102
Duration
5 or 10 days
Language
English or Arabic
Sessions 2027–2030
20 / 9 cities

Overview

Pharmaceutical Quality Assurance is part of the Pharmaceutical & Laboratory track at Garnet Global Training Center. GMP, quality and laboratory programs for pharmaceutical, medical device and testing organisations. The course is taught in English or Arabic as a 5-day or 10-day program, in classrooms in cities such as Dubai, Riyadh, Cairo, London and Istanbul, or live online, and it can be delivered in-house with examples and exercises built around your own operations.

What you will be able to do

  • Explain the principles, terminology and standards that govern Pharmaceutical Quality Assurance.
  • Apply proven methods and tools to real situations from your own workplace.
  • Analyse performance gaps, risks and root causes, and choose the right response.
  • Measure results with practical indicators and report them clearly to management.
  • Leave with a personal action plan you can start using the following week.

Who should attend

QA/QC staff, production and laboratory personnel, regulatory affairs specialists.

Key topics

  • GMP and GLP principles
  • Validation and qualification
  • Documentation and data integrity
  • Deviations and CAPA
  • Regulatory submissions
  • Laboratory instruments

5-day outline

  1. Day 1 Foundations of Pharmaceutical Quality Assurance

    • Scope, terminology and governing standards
    • GMP and GLP principles
  2. Day 2 Methods and tools

    • Validation and qualification
    • Documentation and data integrity
  3. Day 3 Application and case studies

    • Deviations and CAPA
    • Laboratory instruments
  4. Day 4 Performance, risk and compliance

    • Regulatory submissions
    • Measurement and reporting
  5. Day 5 Workshop, assessment and action plan

    • Hands-on workshop on a workplace challenge
    • Final assessment and personal action plan

10-day outline

  1. Day 1 Foundations of Pharmaceutical Quality Assurance

    • Scope, terminology and governing standards
    • GMP and GLP principles
  2. Day 2 Methods and tools

    • Validation and qualification
    • Documentation and data integrity
  3. Day 3 Application and case studies

    • Deviations and CAPA
    • Laboratory instruments
  4. Day 4 Performance, risk and compliance

    • Regulatory submissions
    • Measurement and reporting
  5. Day 5 Workshop, assessment and action plan

    • Hands-on workshop on a workplace challenge
    • Final assessment and personal action plan
  6. Day 6 Advanced techniques and specialist practice

    • Complex cases in depth
    • Common mistakes and how to avoid them
  7. Day 7 Digital tools, data and automation

    • Analysis tools and software
    • Using AI in this field
  8. Day 8 Benchmarking against international practice

    • Global performance benchmarks
    • International case studies
  9. Day 9 Capstone project

    • Analyse a real challenge from your organisation
    • Build the solution and implementation plan
  10. Day 10 Presentations, final assessment and certificates

    • Project presentations and review
    • Final exam and certificate award

Certificate

Participants who attend at least 90% of sessions and complete the final assessment receive a certificate of completion stating 35 contact hours (5-day) or 70 contact hours (10-day).

Schedule 2027–2030

DatesFormatCityLanguageFee (USD)Register
18–29 Jan 202710-day onlineLive onlineArabic5,450Register
14–25 Feb 202710-day classroomRiyadhEnglish8,950Register
10–14 May 20275-day classroomDubaiEnglish4,750Register
5–9 Jul 20275-day onlineLive onlineEnglish2,950Register
3–7 Oct 20275-day classroomMuscatArabic4,750Register
3–7 Apr 20285-day classroomAbu DhabiEnglish4,750Register
15–19 May 20285-day onlineLive onlineArabic2,950Register
19–30 Jun 202810-day onlineLive onlineArabic5,450Register
2–6 Oct 20285-day classroomKuala LumpurEnglish4,750Register
19–30 Nov 202810-day classroomJeddahArabic8,950Register
11–15 Feb 20295-day classroomMuscatEnglish4,750Register
5–16 Mar 202910-day classroomDubaiEnglish8,950Register
2–6 Apr 20295-day onlineLive onlineEnglish2,950Register
9–13 Jul 20295-day classroomIstanbulEnglish4,750Register
1–12 Oct 202910-day onlineLive onlineEnglish5,450Register
20–24 Jan 20305-day classroomCairoArabic4,750Register
4–8 Mar 20305-day onlineLive onlineArabic2,950Register
1–5 Apr 20305-day classroomDubaiEnglish4,750Register
3–14 Jun 203010-day onlineLive onlineArabic5,450Register
1–12 Jul 203010-day classroomViennaEnglish8,950Register

Cities for this course

It can also be delivered in-house in any other city. Request in-house

Frequently asked questions

How long is the Pharmaceutical Quality Assurance course?

It runs as a 5-day program (35 contact hours) or a 10-day program (70 contact hours) that adds advanced techniques and a capstone project.

Where and when is Pharmaceutical Quality Assurance held?

There are 20 public sessions from 2027 to 2030 in cities including Riyadh, Dubai, Muscat, Abu Dhabi, Kuala Lumpur, Jeddah, plus live online. Next dates: 18–29 Jan 2027 (Live online); 14–25 Feb 2027 (Riyadh); 10–14 May 2027 (Dubai).

How much does the Pharmaceutical Quality Assurance course cost?

USD 4,750 for 5 days in a classroom, USD 2,950 for 5 days online, USD 8,950 for 10 days in a classroom and USD 5,450 for 10 days online, per participant excluding VAT.

Is the course available in Arabic and online?

Yes. It is taught in English or Arabic, in a classroom or live online, and materials can be provided in both languages.

Can we run it in-house or customise it?

Yes. We deliver it at your premises in any city and adapt duration, content and examples to your operations.

Do participants receive a certificate?

Yes. Participants who attend at least 90% of sessions and pass the final assessment receive a certificate of completion stating contact hours.