Panel: From Paper to Patient: How Digital Product Information is Reshaping Access and Trust in Medicines

This session explores how digital health tools and regulatory innovation are transforming pharmaceutical packaging; shifting from traditional paper leaflets to electronic product information (ePI). With a strong focus on the European regulatory environment, the panel will discuss how ePI is unlocking smarter, more sustainable, and patient-centric approaches to packaging and medicine information delivery.

Key Takeaways for R&D and Manufacturing Teams:

Understand the EU’s regulatory shift toward ePI and its impact on packaging requirements, batch release processes, and lifecycle management.

Learn how replacing paper leaflets with digital alternatives can streamline multilingual packaging, reduce manual errors, and support regulatory compliance.

Explore how ePI enables more flexible packaging strategies—minimising overproduction, reducing material waste, and accelerating time-to-market for multilingual SKUs.