Regulatory Information Management System (RIMS) Roundtable

Regulatory departments are the brains within the pharmaceutical industry. You are ultimately responsible for the life of your company’s assets. Not only do you have very high standards of regulations that must be followed, you also have to coordinate complex activities with multiple stakeholders to ensure medicines can be assessed effortlessly for quality, efficacy and patient safety.

In this RIMS Roundtable we will discuss these challenges and show you practical solutions to make your life easier.


Hotel Bergström, Lüneburg, Germany

Next airport is Hamburg.

Agenda 18 October

19:00h Welcome Dinner (optional)

Agenda 19 October

08:30-08:45h Welcome and Introduction - Maximilian Munte, EXTEDO

08:45-09:30h Regulatory Information Management – Challenges and Opportunities - David Kološić, ASPHALION

09:30-10:00h Best Practices Based on a Customer Case -  Kashmira Gupte, EXTEDO

10:00-10:30h Coffee Break

10:30-10:45h RImanager Live Demo - Anjana Pindoria, EXTEDO

10:45-12:00h Interactive Session: Journey of the Drug / Challenges of Planning & Tracking (Serialisation, Labelling) - Anjana Pindoria, EXTEDO

12:00-13:00h Lunch (optional)

Registration and Details

(Participation is free of charge)