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The Schlafender Hase Team

E-PIL Legislation: The Impact on Patient Safety, Accessibility and Environmental Sustainability

Providing patients and Health Care Practitioners with electronically delivered e-Labelling is becoming increasingly important. Several Regulatory Authorities now permit and encourage online e-PIL content, with other regions following suit.
Original Broadcast Date: April 27, 2022
Duration: 1 hr 11 min

Ensuring content is delivered accurately in print and online formats, will be vital to ensuring patient safety, especially during the complex transition phase from printed-paper to electronic patient information.

With accessibility high on the agenda, the evolution of e-PILs will rapidly progress from flat pdf facsimiles of the printed insert leaflet, into interactive audio-visual presentations of information and therefore should be planned for within any e-PIL strategic initiatives.

The ultimate benefit to both patient and planet is easily demonstrated, however the changes and impacts across life sciences’ businesses will undoubtedly be challenging.

Key Learning Points:

Upon the conclusion of this webinar you will be able to: 

  • Understand the latest country Regulations & Guidance initiatives

  • Identify the impact on your current Labelling and Artwork processes

  • Begin implementing actionable strategies for:

    • Accurate content – The foundation of Consistent & Compliant e-Labelling

    • Right-first-time Transformation & File distribution

  • Identify impacts on Patient Safety & Sustainability

  • Recognize future benefits of an e-PIL strategy for your organization

Who Should Attend:

  • RA Med Dev

  • RA Pharma

  • Medical/Technical Writers

  • Reg. Ops

  • Labelling

  • Quality Management


Ashley Goldie
Aultra, Ltd.

Ashley Goldie is an experienced, detail-oriented professional and motivational leader, adept at working across the labelling and packaging creation process within the life sciences sector. He is practiced in improving operational performance and leading enterprise labelling technology companies. Goldie is knowledgeable in trend research, printed packaging, online content and directing activities to achieve extraordinary results.


Do you want to find out more about how your proofreading life can be easier? Get in touch and we’ll tell you all about it.

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January 17, 2024

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TOPRA Sponsored Webcast: A Non-Technical AI Introduction for Regulatory Affairs Professionals

AI is already being used in many Life Science applications, meanwhile Health Authorities are looking to regulate the use of AI. As a regulatory affair professional, it is essential to have an understanding of this technology.    In this general introduction to the field of AI, different uses of the term "Artificial Intelligence" will be discussed, and which might be desirable in a given context. 

August 23, 2023

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Join Schlafender Hase on September 14th, as we guide you through the typical steps needed to properly identify the right tool for your organization and how to get it approved.

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Digital transformation is all the rage these days, but what does that actually mean for professionals working with regulated content in Pharma and Med Device, and more importantly, what does it mean for you? Join us on November 10th as we explore the why and how of a digital proofreading workflow.