GarnetGlobal Training Center العربية

Pharmaceutical & Laboratory

Pharmacovigilance

اليقظة الدوائية

Download brochure (PDF) البروشور بالعربية PDF

Code
GGT-PH-106
Duration
5 or 10 days
Language
English or Arabic
Sessions 2027–2030
20 / 9 cities

Overview

Pharmacovigilance 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 Pharmacovigilance.
  • 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 Pharmacovigilance

    • 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 Pharmacovigilance

    • 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
4–8 Jan 20275-day classroomLondonEnglish4,750Register
15–19 Feb 20275-day onlineLive onlineEnglish2,950Register
3–14 May 202710-day onlineLive onlineArabic5,450Register
14–18 Jun 20275-day classroomDubaiArabic4,750Register
5–16 Sep 202710-day classroomJeddahArabic8,950Register
3–7 Jan 20285-day onlineLive onlineEnglish2,950Register
20 Feb – 2 Mar 202810-day classroomDohaEnglish8,950Register
15–19 May 20285-day classroomSingaporeEnglish4,750Register
14–25 Aug 202810-day onlineLive onlineArabic5,450Register
10–14 Sep 20285-day classroomRiyadhEnglish4,750Register
8–12 Jan 20295-day classroomAbu DhabiArabic4,750Register
5–9 Mar 20295-day onlineLive onlineArabic2,950Register
18–22 Jun 20295-day classroomLondonEnglish4,750Register
17–28 Sep 202910-day classroomDubaiEnglish8,950Register
8–19 Oct 202910-day onlineLive onlineEnglish5,450Register
11–15 Mar 20305-day classroomAbu DhabiEnglish4,750Register
15–26 Apr 203010-day onlineLive onlineEnglish5,450Register
6–10 May 20305-day onlineLive onlineArabic2,950Register
5–16 Aug 203010-day classroomGenevaEnglish8,950Register
15–19 Dec 20305-day classroomKuwait CityEnglish4,750Register

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 Pharmacovigilance 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 Pharmacovigilance held?

There are 20 public sessions from 2027 to 2030 in cities including London, Dubai, Jeddah, Doha, Singapore, Riyadh, plus live online. Next dates: 4–8 Jan 2027 (London); 15–19 Feb 2027 (Live online); 3–14 May 2027 (Live online).

How much does the Pharmacovigilance 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.