| VPD-SYM-2011-SESS-1 |
Symposium 2011 Session 1 |
£60.00 |
|
| VPD-SYM-2011-DEV-SESS-1 |
Symposium 2011 Devices Session 1 |
£60.00 |
|
| VPD-SYM-2011-SESS-3 |
Symposium 2011 Session 3 |
£60.00 |
|
| VPD-SYM-2011-SESS-4 |
Symposium 2011 Session 4 |
£60.00 |
|
| VPD-SYM-2011-SESS-6 |
Symposium 2011 Session 6 |
£60.00 |
|
| EMA10SESSION8 |
The Centralised Approval Process - Knowing the rules to navigate successfully |
£50.00 |
|
| SYM10SESSION2 |
Scientific Advice Session at the 7th TOPRA Symposium London |
£50.00 |
|
| SYM10SESSION4 |
Globalisation of Pharmaceutical Regulation – What do Agencies Discuss behind Closed Doors? |
£50.00 |
|
| VPD-021209-S7 |
Joint TOPRA-EMA meeting - New European Variations Legislation and Guidelines |
£50.00 |
|
| VPD-20090915-IN |
Paediatrics 2009 Introduction |
£0.00 |
play video
|
| VPD-20090915-S1 |
How to prepare the submission dossier? Procedural and scientific advice - practical aspects - Péter Károlyi, Scientific Administrator, EMEA |
£40.00 |
|
| VPD-20090915-S2 |
The Paediatric Regulation, an industry viewpoint based on experience from Novo Nordisk A/S - Vibeke Bjerregaard, Novo Nordisk A/S, Denmark |
£40.00 |
|
| VPD-20090915-S3 |
Part C, D and E: Waivers, Study Plans, Deferrals - Where things can go wrong, potential problems and how to avoid them - Jan Gross, Merck Serono, Germany |
£40.00 |
|
| VPD-20090915-S4 |
PIP Modification and Compliance - experiences to date - Péter Károlyi, EMEA & Lisette Vromans, Schering Plough, The Netherlands |
£40.00 |
|
| VPD-20090915-S5 |
Reports from Workshops - Moderated by Sonja Pumpluen, Head Global Drug Regulatory Affairs, Actelion, Switzerland |
£40.00 |
|
