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)