Advanced Stability Testing of Pharmaceuticals MasterClass - US edition

24-27 February, 2026

Increase the likelihood of studies receiving regulatory approval

A series of practical exercises will take place throughout the programme to give participants the opportunity to apply their knowledge under the guidance of our experienced trainer.

24-27 February, 2026, Virtual

STARTING TIME 08:00 A.M. EST | 05:00 A.M. PST | 13:00 UTC | 14:00 CET

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Key learnings

Knowledge

Gain knowledge on storage tests, conditions and protocols

Stability Requirements

Comply with stability requirements for new and existing drug substances, products and line extensions

Learn

Learn how to design highly efficient protocols for global marketing with potentially large financial savings

Discover

Discover how to manage stability samples and facilities

Understand

Understand what stability testing is required following changes to a product

Discuss

Discuss data treatment, shelf-life assignment and extrapolation

Trusted by over 17,000 delegates across leading companies

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Overview

By attending this intensive two-day seminar, delegates will learn how to:

-Carry out appropriate stability studies and manage stability samples and facilities
-Design stability studies that are suitable for global marketing
-Increase the likelihood of studies receiving regulatory approval
-Save resources on stability testing with potential large financial savings

A series of practical exercises will take place throughout the programme to give participants the opportunity to apply their knowledge under the guidance of our experienced trainer.

#masterclass #glceurope #pharma #globaltraining #stabilitytestingpharmaceutical

Trainer

Paul R Palmer

Managing Director
Pharma Quality Services Limited (PQSL)

Paul R Palmer is a Director / Pharmaceutical Consultant and a practicing EU / UK Qualified Person. He has over 35 years experience in the pharmaceutical industry in the development, manufacture and supply of medicinal products and medical devices. Throughout his career, Paul has intentionally taken on all opportunities as they arose in order to develop a broad range of knowledge with an in-depth detailed understanding of manufacturing, storage, distribution, research, computerised systems, as well as the facilities and services to support each.

People and systems have always been a core focus, how to ensure best use, optimise and enhance efficiency. He has a level of curiosity rarely displayed in people taking on the qualified person role in pharmaceutical manufacturing. Culture, behaviour and psychology are all significant influences on the systems and processes we implement, but are often ignored.

Paul studied psychology as part of his MSc in 1993 and has always enjoyed observing the world around him with a curiosity that is rarely satisfied.

Farah Nadeem

Farah Nadeem is an Operations Manager at Paul R. Palmer Limited, a Pharmaceutical Consultant, and a Trainee Qualified Person. A Pharmacist and recognised QA expert, she has over 20 years of experience in the development, manufacture, and supply of medicinal products. She has held multiple quality assurance roles, gaining broad expertise in manufacturing, storage, distribution, and the supporting facilities and services. Her experience includes documentation management - writing, reviewing, and auditing SOPs and QMS implementations, and helping companies meet regulatory requirements. In her current role, Farah supports clients in obtaining MIA(IMP) and MIA licences, preparing for and hosting regulatory inspections, and delivering services such as QP declarations for API manufacturers, batch release (commercial and clinical), compliance audits, and GxP coaching and training.

Aneta Jell

Aneta Jell is a seasoned Quality Assurance professional with over 20 years of experience across manufacturing, contract operations, and quality leadership in the pharmaceutical industry. Currently serving as Quality and training manager at Paul Palmer limited she oversees global contract manufacturing quality, ensuring GxP compliance, regulatory alignment, and supply chain integrity. Her expertise spans GMP, ISO 9001, ISO 17025, and QMS administration, with proven strength in audits, CAPA, deviations, and technical agreements. A qualified QMS lead auditor with bilingual proficiency in English and Slovak, Aneta is recognised for driving continuous improvement, fostering compliance culture, and leading high-performing quality and HSEteams.

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Reasons to attend a masterclass

Practical knowledge

Venture into undiscovered territories and gain inspiration through collaboration

Interactivity

Boost your professional skills by directly engaging with domain experts

World-class trainers

Gain value and learn from the best instructors

Networking

Build a top-notch community and advance your career

Who should attend img WHO SHOULD ATTEND

-Quality assurance
-Qualified Person
-Stability Unit
-The management of stability samples and facilities
-Quality Unit Head
-Analytical Laboratory Head
-Pharmaceutical Product Development Leader

Ticket options for you

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Testimonial

Our success stories

"High attention to detail in course content and very well delivered"

Simon Halsey

Product Development Manager
Essentra Packaging
United Kingdom

Our success stories

"Very good training led by two knowledgeable and open experts. Excellent insight given on many complex topics. Interactive and highly useful"

Aurelie Vivicorsi

USP PD Team Manager
Celonic AG
Switzerland

Our success stories

"Great course, impressed with the knowledge of the trainers and ability to answer wide variety of questions!"

Emilia Szwej

Manager, Senior Investigator
MT Sword Laboratories (BMS)
Germany

About GLC

Global Leadership Conferences began as an ambitious dream by three founders ten years ago. Today its an international series of interactive events, exploring the hottest topics in critical fields. Each year, thousands of professionals join us to challenge the status quo and learn innovative ways to create new solutions in Finance, Pharmaceutical, HR, Health & Safety, and Energy.

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