European HTA - What have we learned, what lies ahead?
Free Webinar on 4th of May 2022
Join us as we share our experiences and learnings fromEUnetHTA Joint...
FEB 24 2022 Webinar: Real World Data
New Frontiers in the RWD and Current Use-Cases for RWD Collection
Powered by AMS and Glatt Pharmaceutical Services
Fewer than...
Online Course: Update Medical Device Regulation
AMS developed together with KKS Heidelberg, Department for Advanced Training and Metecon GmbHDepartment for...
CTR and the CTIS - Clinical Trials Information System
The Clinical Trial Regulation (CTR) will come into force on 01 Feb 2022. The CTIS submission platform...
EU HTA – Health Technology Assessment across Europe
How to bridge the gap between EUnetHTA's cessation and an EU Regulation's application?
Considering the fact that EUnetHTA...
10 Jahre AMNOG - Rückblick und Ausblick
Dieses Jahr wird das 10-jährige Bestehen des Arzneimittelmarkt-Neuordnungs-Gesetzes AMNOG gefeiert. Als Dienstleister der ersten...
EUnetHTA’s Joint Action 3 has been prolonged to May 31, 2021. After a temporary suspension of Early Dialogues (ED) due to the current pandemic situation, ED...
Profit from the simultaneous feedback of regulatory and HTA bodies in order to generate your data set in the most efficient way!
What is new?
EMA and EUnetHTA have...
Um Kooperationen auszuzeichnen und Partner entsprechend zu honorieren, verleiht AbbVie Global jährlich den Preis 'Supplier of the Year'. Kriterien, um für den...
AMS electronic Patient Reported Outcomes (AMS-ePRO®)
AMS-ePRO® supports Clinical Research
You can now capture your patients data Anytime Anywhere with...