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Rare diseases

Expansion into new international biotech markets can be challenging. Unfamiliar regulations and licensing, coupled with language and cultural differences, can all be barriers to growth. If you’re considering venturing into Europe and beyond, our easy-to-follow guides, shaped by 30 years of expertise in the rare disease market, will assist you in navigating challenges and gaining a profound understanding of the complexities involved in launching orphan drugs into new markets. To learn more about how Sciensus can facilitate and support your Europan expansion, visit: Rare Diseases and Orphan Drugs

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Thought Leadership, Rare diseases

Expand into Europe: unlocking the orphan drug market

News, Rare diseases

Rare disease day 2025

Thought Leadership, Rare diseases

Beyond compliance: unlocking the strategic potential of PASS in rare disease therapy  

World Orphan Drug Congress USA

Events, Rare diseases

World Orphan Drug Congress USA 2025

Blogs, Rare diseases

The developing role of gene therapy in finding solutions to rare diseases    

EAP launch

Blogs, Rare diseases

Strategic timing: When should biotech firms consider launching expanded access programs?   

patient-reported data

Blogs, Rare diseases

How to set up an EAP without a European presence 

Expanded Access Programs

Blogs, Rare diseases

EMA orphan drug designation

real-world data

Blogs, Rare diseases

Four considerations before collecting real-world data in your EAP

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