17 September 201517:00–21:30 (CEST)PSE Building D – EPFL Room PLUTON1015 Lausanne
Join regulatory colleagues from across Switzerland for an evening of networking and speaker presentations. The presentations will cover preclinical /toxicology requirements for an IND/CTA submission and duties of the Qualified Person (QP) in Europe (CTA, MAA and beyond).
Do not miss this unique opportunity to interact with other regulatory professionals from your region. Refreshments will be available for all and participants are eligible to claim two continuing education and/or RAC recertification credits. Certificates of Attendance will be provided to program attendees. This event is hosted by the RAPS Switzerland Chapter and is intended to promote networking among local regulatory professionals.Scheduled presentations include:• Non-clinical safety requirements before FIH Clinical Trial – Hasnaa Haddouk, toxicologist, AC Immune SA• The Qualified Person – Claude Ammann, CA Consulting (TBC)