Lung cancer drug taken off German market because of no additional benefit rating
On 25 August 2022, Janssen has announced that they have withdrawn the lung cancer drug Rybrevant (amivantamab) from the German market with
German Market Access – Simplified
Everything you need to know in one place, explained in simple terms
On 25 August 2022, Janssen has announced that they have withdrawn the lung cancer drug Rybrevant (amivantamab) from the German market with
Currently, reserve antibiotics are excluded from a benefit assessment by the G-BA. The G-BA decides whether to accept a new antibiotic onto the
In this post, I’m following up on the key points on the real-world evidence (RWE) data collection in Germany with an IQWiG
In this post, I’ll summarise the key points on the real-world evidence data collection in Germany, that the G-BA can request since
Welcome to the last post in the HTA series, focusing on the changes to HTA and early benefit assessments in Germany in
Welcome! In this post, I am going through the steps on how the G-BA chooses the appropriate comparative therapy (ACT). I conclude
This week, we are having a brief look at two brief reports on PROs recently published by the IQWiG. We’ll cover: As
Welcome, this week’s post on the G-BA’s views on endpoints is the second article in the benefit assessments series. You’ll learn about:
This is the first article in a series about maybe the most important topic influencing market access in Germany: HTAs or early
In July 2021, we had heard that the G-BA had agreed to joint EU HTAs coming to Germany. Now, on 14 December