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...

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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...

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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...

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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 ...

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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...

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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...

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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 ...

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Articles
10.09.2024
Strategic approaches to achieving HTA approval for...

Achieving HTA approval for orphan drugs requires strategic planning, early engagement, strong eviden...

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Articles
28.08.2024
How to integrate Market Access strategy with evide...

Introduction What is the secret to a successful drug launch? One crucial factor is establishing a cr...

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Articles
20.08.2024
Adapting to the EU HTA: how to restructure your Ma...

Our latest article discusses key strategies for pharma manufacturers' commercial readiness for EU HT...

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