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Additional Risk Minimization Measures (aRMMs) and Their Effectiveness Training Course

Delve into the world of additional Risk Minimization Measures (aRMMs) and explore everything from the regulatory framework surrounding aRMMs to their impact on patient safety and healthcare outcomes.

9 April 2025
+ 10 September 2025, 3 December 2025 »

from £350

Need help?  Enrol/reserve

Course overview

This course delves into the world of additional Risk Minimisation Measures (aRMMs), providing a thorough understanding of their development, implementation and assessment. Participants will explore the regulatory framework surrounding aRMMs, learn how to design effective risk minimisation strategies and evaluate their impact on patient safety and healthcare outcomes. This course combines theoretical knowledge with practical insights, enabling attendees to enhance their skills in managing and monitoring aRMMs in their organisations.

This course is part of our Vigilance training course collection; for information on the basics of PhV, consider taking a look at our beginner-friendly Pharmacovigilance training course.

Benefits of attending

  • Gain in-depth knowledge of aRMMs, including their purpose, development and regulatory requirements
  • Learn how to create and implement effective risk minimisation strategies tailored to specific safety concerns
  • Discover methods for assessing the effectiveness of aRMMs and making data-driven improvements
  • Stay informed about the latest regulatory guidelines and best practices for aRMMs
  • Explore the ethical aspects of implementing aRMMs and ensuring patient safety

Who should attend?

  • Pharmacovigilance specialists
  • Drug Safety Officers
  • Regulatory affairs professionals
  • Clinical research associates
  • Medical affairs personnel
  • Risk management professionals
  • Healthcare Quality Assurance specialists

Enrol/reserve

This course will cover:

Introduction to aRMMs

  • Overview of additional Risk Minimisation Measures
  • Importance and objectives of aRMMs and their effectiveness evaluation

Understanding global regulatory guidelines for aRMMs

  • Key regulatory requirements and compliance
  • How new safety data affect decisions and benefit-risk balance   

Principles of designing risk minimization strategies

  • Designing Effective aRMMs
  • Case study on aRMM implementations

Practical approaches to implementing aRMMs

  • Implementation Strategies: Engaging stakeholders and ensuring adherence
  • Real-world scenarios and problem-solving

Methods for monitoring and assessing the impact of aRMMs

  • Data collection, analysis, and reporting
  • Ethics in aRMM Implementation

Enrol/reserve

Alina Panourgia
Composite Pharma

Alina Panourgia is an experienced QA/PV Auditor and Regulatory Affairs professional, with a career spanning various regions.

Alina started her career in SEA working at the manufacturing site leading Quality Control/Regulatory Affairs department. She still prepares companies for inspections and provides trainings.

Since relocating to the Middle East in 2015, Alina has worked as a freelancer, collaborating with UK, US and EU companies on PV projects. Additionally, Alina has overseen regulatory submissions and pharmacovigilance activities in the MENA, LATAM and CIS regions.

Alina is a frequent speaker at international forums, conferences and training programs, sharing her expertise on various topics in pharmacovigilance, regulatory affairs and quality improvements.

She has presented at GCC Regulatory Affairs/PV Summits, Drug Safety Symposiums and other significant industry events within MENA region.

More details

NEW higher discounts for multiple bookings - bring your colleagues to make your training budget go further:

  • 30% off the 2nd delegate*
  • 40% off the 3rd delegate*
  • 50% off the 4th delegate*

Please contact us for pricing if you are interested in booking 5 or more delegates

9 April 2025

Live online

09:00-12:30 UK (London) (UTC+01)
10:00-13:30 Paris (UTC+02)
04:00-07:30 New York (UTC-04)
Course code 15386

  • GBP 350 400
  • EUR 490 560
  • USD 562 640

Until 05 Mar

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Not ready to book yet?

for 7 days, no obligation

10 September 2025

Live online

09:00-12:30 UK (London) (UTC+01)
10:00-13:30 Paris (UTC+02)
04:00-07:30 New York (UTC-04)
Course code 15387

  • GBP 350 400
  • EUR 490 560
  • USD 562 640

Until 06 Aug

View basket 

 
Not ready to book yet?

for 7 days, no obligation

3 December 2025

Live online

09:00-12:30 UK (London) (UTC+00)
10:00-13:30 Paris (UTC+01)
04:00-07:30 New York (UTC-05)
Course code 15388

  • GBP 350 400
  • EUR 490 560
  • USD 562 640

Until 29 Oct

View basket 

 
Not ready to book yet?

for 7 days, no obligation

* Early booking discounts may not be combined with other discounts or offers. As such, the discounts for 2nd/3rd/4th delegates are based on the full price; and apply only when booking multiple delegates on the same date.

Denmark

  • 2care4 Generics ApS

Enrol/reserve

Multiple colleagues? See above for details of our discounts for 2, 3, or 4 delegates. For more, talk to one of our training experts to discuss how to:

Run this course conveniently and cost-effectively in-house for your staff and colleagues

Aleksandra Beer

Aleksandra BEER
Training expert

Yesim Nurko

Yesim NURKO
Training expert

+44 (0)20 7749 4749

inhouse@ipi.academy