Biosimilars 2017
Termindetails
Wann
22.06.2017 um 15:30
Wo
Kontakttelefon
Teilnehmer
Those working in the following areas will particularly benefit from this event:
- Marketing authorisation
- Clinical and preclinical development
- CMC/quality and analytics
- Market access and business development
- Legal affairs/patent protection
Do you work in biosimilars or intend to do so? Then you should not miss this conference with leading biosimilars experts. During the two conference days, you will receive a full update from development requirements, to marketing authorisation requirements through to reimbursement topics. I would be very pleased to welcome you on the 21st June at the conference! Dr Henriette Wolf-Klein Department Manager Pharma & Healthcare
- Substitution and interchangeability
- current status in Germany, the EU and the US
- Extrapolation of indications - remaining challenges
- SPC and patents - managing product protection life cycles
- Key considerations for combination products
- Analytical development and comparability exercises