Dr. Penelope Gallinger
IQVIA Commercial GmbH & Co. OHG, München, Germany
Principal Market Access und HTA
RWAS Real-World & Analytics Solutions
More information please click here.
Dr. Martin Granser
Roche Pharma AG, Grenzach-Wyhlen
Head Strategic Pricing & Reimbursement
More information please click here.
Dr. Vanessa Elisabeth Schaub
F. Hoffmann-La Roche Ltd, Basel, Switzerland
Head Global & EU HTA Strategy
27/11/2024
27/11/2024
9:00 am - 5:00 pm seminar
You may dial in 30 minutes in advance
online
online
Event - 1,190 € plus tax
The participation fee includes documentation for download, a certificate, access to the Learning Space and technical support including PreMeeting.
Event - 1,190 € plus tax
The participation fee includes documentation for download, a certificate, access to the Learning Space and technical support including PreMeeting.
Dr. Henriette Wolf-Klein
Head of Department
+49 6221 500-680
h.wolf-klein@forum-institut.de
This seminar will focus on AMNOG and JCA dossier preparation as well as the German AMNOG procedure in comparison with the EU HTA procedure.
Are you involved in the market access of innovative drugs in Germany? Do you need to understand the main principles involved, especially in comparison with the upcoming EU HTA procedure?
Then this seminar will familiarise you with the main tasks and hurdles along the way. Three outstanding market access experts will guide you through the procedure and can answer your questions on both the national and the EU level.
09:00 Welcome and introduction
09:15
Dr Penelope Gallinger
10:15 Short break
10:25
Dr Penelope Gallinger
11:30 Coffee break
11:45
Dr Penelope Gallinger, Dr Vanessa Elisabeth Schaub
13:00 Lunch break
14:00
Dr Penelope Gallinger, Dr Martin Granser
15:45 Coffee break
16:00
Dr Vanessa Elisabeth Schaub
17:00 End of seminar
of 5 stars of all ratings from 2023
of 5 stars on Trustpilot = good
Are you new to pharmacovigilance and looking to kick-start your career? Then this online course is just for you. Gain a ...
Online seminar on Market Access & Pricing in Europe - this is how you can gain access as a pharmaceutical manufacturer!
To make the most of ICH Q12 opportunities, you have to be aware of the relation between ICH guidelines Q8 to Q12 and how...
This course familiarises you with regulatory post-approval duties and provides first-hand information on variation submi...
- GVP Module XVI Risk minimisation measures (Rev 3) came into force - Do you already have a good understanding of PSUR a...
Are you interested in our international continuous education programme? We provide a variety of specialised courses.
DetailsWe are now officially certified to ISO 9001 and ISO 21001 standard.
DetailsMore than 4,500 customers have rated our training courses. Thank you for awarding us 4.3 stars out of 5.
Details