Good Clinical Practice: An expert guide

Friday 19th June 2026 13:00 - 14:00 (BST)


Understand the key changes in ICH-GCP E6(R3) and what they mean for clinical research and the evolving MSL role


Masterclass Details:

The revision of ICH-GCP E6(R3) marks an important evolution in the framework guiding global clinical research. As clinical trials become increasingly complex and technology-driven, the updated guideline introduces a more flexible and risk-based approach while maintaining the highest standards of patient safety and data integrity.

This 60-minute masterclass will provide those working in medical and clinical functions a clear and practical overview of the revised framework and the thinking behind the update. Attendees will gain insight into how the new guideline aims to support modern clinical trial delivery while strengthening quality management across the research lifecycle.

Nelle Stocquart, Clinical Research & GCP Training Specialist, will explore the key differences between ICH-GCP E6(R2) and E6(R3), highlighting the updated principles, broader scope, and the evolving responsibilities of stakeholders involved in clinical research.

The session will also examine the international implementation landscape and what organisations across the Life Sciences industry should consider as regulators and sponsors begin preparing for adoption.

 


Join live to gain a practical introduction to the evolving GCP landscape and what it means for clinical research.


 

Key Learning Objectives:

  • Understand the rationale behind the revision of ICH-GCP E6(R3)
  • Identify the key differences between ICH-GCP E6(R2) and E6(R3)
  • Explore the updated principles and expanded scope of the revised guideline
  • Understand the roles and responsibilities of MSLs and other stakeholders in clinical trials under the new framework
  • Gain insight into the international implementation landscape and what the changes may mean for the Life Sciences industry

LSAA reserves the right to restrict access to this webinar to LSAA and MSLA members.

 

  • Date and time

    19th Jun 2026 13:00 – 14:00 (BST)

Testimonials

Logo of Louise Rudd, Senior Medical Science Liaison
Louise Rudd, Senior Medical Science Liaison

Novartis UK

“The MSLA is a priceless resource for all MSLs and aspiring MSLs. The content of the webinars has been incredibly well thought out, it’s relevant, stimulating and you get this all for free!

I’m proud to be a part of the community and I have met some amazing people that have helped me grow as an MSL.”

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Danny Burney, Field Medical Lead

Bristol-Myers Squibb

“Being part of the MSLA has given me a real sense of connection with peers who understand the challenges and opportunities of medical leadership and MSL roles alike.

The open exchange of ideas, expert insights and supportive community have all been incredibly valuable -it’s an inclusive community space that genuinely helps you grow, stay inspired, and enhance your impact within Medical Affairs.”

Logo of Stuart Hill, Medical Director
Stuart Hill, Medical Director

Merck Group

“Membership of the MSL Association gives everyone who is an MSL or an aspiring MSL, access to an invaluable series of resources that can really enhance your knowledge, skills and development to the next level, to allow you to be the best that you can be. It is a must for everyone.”

Logo of Vanesa Salazar, Researcher & Aspiring MSL
Vanesa Salazar, Researcher & Aspiring MSL

The University of Edinburgh

“Being part of the MSLA has been incredibly valuable in my transition from academic research to Medical Affairs. Through the masterclasses, networking and mentoring opportunities, I’ve gained a clearer understanding of the MSL role and the skills needed to succeed.

The MSLA has also helped me stay up to date with the latest trends and challenges in the field as the role keeps evolving.

Lastly, through MSLA I could connect with professionals from different seniority levels and diverse backgrounds that inspired me and supported me during this journey.”

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