Sponsored Webcast: E-Labeling and What it Means for Regulatory Teams (On Demand)
E-labeling is no longer a future concept. Regulatory agencies worldwide, including the EMA, FDA, and MHRA, are advancing digital product information initiatives. But what does this mean for your daily work as a regulatory professional? How will your submission and labeling processes change? And how can you prepare today to avoid last-minute compliance risks?
Join us for this practical webinar to gain clarity on the changes you can expect with digital product initiatives and learn how you can make the transition smoother. Don't wait until e-labeling is mandatory
Registration Fees & Deadlines
Member: $ 0| Nonmember: $50
Learning Objectives
- Understand the global shift to e-labeling.
- Why regulators are pushing for it and what’s happening in key markets like the EU, US, and UK.
- Explore how e-labeling will impact your daily work.
- What’s changing in submission workflows, approval processes, and content management.
- Use Case Spotlight: Learn how Rote Liste supports converting existing pharmaceutical data into structured ePI content, ensuring compliance with EMA guidelines.
Who Should Attend?
Regulatory Affairs Professionals
Audience Learning Level
Basic: Content is introductory in nature and requires no requisite knowledge or experience to grasp concepts and related exercises. Basic educational activities are meant to establish a foundation of knowledge and/or competence that will be expanded upon in practice or in higher level activities.
Speakers
Mike Baird
Schlafender Hase, Director of Product Management
Josephine Bergmann Paslat
Rote List, Pharmaceutical Product Owner Industry Solutions
Carina Bachman
Rote List, Pharmacist, Editorial Team
Proof of Attendance
A certificate of attendance can be downloaded from the RAPS Learning Portal following the event.
