23rd Regulatory Affairs Conference by Medicines for Europe

Attendees of the 23rd Regulatory Affairs Conference can look forward to a varied program presented by industry experts, leading regulators, and European institution officials. They all come together in Amsterdam, in the Netherlands, to discuss the latest developments in the regulatory environment and their upcoming impact on everyday regulatory tasks. Here, the participants can update their knowledge of artificial intelligence (AI), big data, or environmental risk assessments and prepare their respective organizations for future implications. 

Meet the EXTEDO team at our booth and use the opportunity to discuss your regulatory processes with our experts. With Rote Liste Service GmbH, we bring you even more knowledge regarding the electronic processing of regulated information for healthcare professionals and patients. 

And there is even more - we are happy to send Anjana Pindoria-Rettenberger, Director of Product Strategy, as an expert speaker!

Make sure to mark your calendar and join Anjana in her session: 

Date: Thursday, 27  February 2025
Time: 14:15 - 15:45 CET

Session 3: Regulatory affairs fitting with the digital age – what is the journey and how to be prepared?

Chaired by Remco Munnik, Chair of Telematics Working Group, Medicines for Europe, Deloitte, this session explores the evolving role of digitalization in the regulatory processes. Moving towards a structured data-driven ecosystem, this discussion with a horizontal focus brings together experts with different backgrounds: PMS, ESMP, ePI project, and the eCTD 4.0 pilot. Its goal: Nothing less than to better understand the challenges faced by all the parties involved in the different stages of the process.

Anjana Pindoria-Rettenberger,  Director of Product Strategy