Search results for: rare disease

ATMP pricing landscape: why traditional models bre...

A €3 million invoice for a single infusion can dazzle as easily as it alarms. Gene therapies such ...

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From submission to guidance: Demystifying the NICE...

The vast majority of products launching in the UK will be assessed by the National Institute for Hea...

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Engaging Stakeholders: The Power of Patient and Cl...

Decisions regarding National Institute for Health and Care Excellence (NICE) appraisals are not made...

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NICE 2025 Update: How New Appraisal Reforms Impact...

The National Institute of Health and Care Excellence (NICE) has published several updates and releas...

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Avoiding pitfalls: Top 5 reasons NICE HST/STA subm...

Most pharmaceutical products hoping to launch in the UK will be assessed by NICE as a Single Technol...

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Mastering NICE submissions: The three pillars for ...

Securing a positive recommendation from the National Institute for Health and Care Excellence (NICE)...

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HST or STA? Navigating NICE’s Dual Pathways for ...

When bringing a new health technology to market in England, pharmaceutical and biotech companies mus...

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EU Pharma Package Overhaul: Council Agreement Ushe...

Executive Summary  What Has Changed in the Pharma Package?  The Council’s agreed text on the Pha...

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Joint Scientific Consultations: When, Why, and How...

The increasing complexity of bringing innovative therapies to market across various jurisdictions pr...

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Unlocking Payer Confidence: Why Early HTA Scientif...

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

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