Articles
19.05.2025
Avoiding Common Pitfalls in HTA Scientific Advice:...

With the implementation of the EU HTA (Regulation (EU) 2025/117) and ongoing adaptation of methods u...

Read more
Articles
12.05.2025
Driving Internal Alignment: How Early HTA Advice U...

As the regulatory and market access landscape continues to evolve across Europe, timely and strategi...

Read more
Articles
07.05.2025
Unlocking Payer Confidence: Why Early HTA Scientif...

In the current pharmaceutical environment, obtaining regulatory approval is no longer enough to ensu...

Read more
Articles
23.04.2025
EU HTA Regulation for Medical Devices Starts in 20

The long-anticipated EU Health Technology Assessment (HTA) Regulation (Regulation (EU) 2021/2282) wa...

Read more
Articles
07.04.2025
Reforming Health Technology Assessments to Embrace...

The advent of cell and gene therapies (CGTs) represents a paradigm shift in medicine, offering the p...

Read more
Articles
17.03.2025
PICO and Mix: What the PICO exercises mean for JCA...

The population, intervention, comparator, and outcomes (PICO) element of the upcoming EU Joint Clini...

Read more
Articles
26.02.2025
World EPA 2025: Evaluating the capabilities of AI ...

AUTHORS: Julia Tokarska, Ella Odams, Richard Sloggett, Graham Foxon OBJECTIVES  To evaluate if ...

Read more
Articles
25.02.2025
How are countries implementing the EU HTA Regulati...

EU HTA Regulation goes live: A new era for HTA begins  The much-awaited implementation of the r...

Read more
Articles
10.12.2024
A 2024 update: Is NRDL inclusion in China really t...

The National Healthcare Security Administration (NHSA) of China completed its annual review of the N...

Read more
Articles
17.09.2024
Can Real-World Evidence overcome uncertainty in Ra...

We examine how real-world evidence strategies help address uncertainties in rare disease treatments ...

Read more

Stay in the know, subscribe to our newsletter

Be the first to receive exclusive content on the latest from the pharmaceutical and market access sector.