Your Trusted Gateway to the European Pharmaceutical Market
Fast and Affordable
Work with us to create an extraordinary business
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★★★★★
4.8 rating from 100+ customers
Introducing Eurosia Pharma
Eurosia Pharmaceutical Limited based in Ireand, Eurosia Pharmaceutical Limited specializes in providing efficient and cost-effective regulatory and market access solutions for pharmaceutical companies aiming to establish a presence across Europe.
We support your success with end-to-end services that include:
Regulatory Strategy & Dossier Services
From initial gap analysis to full CTD dossier preparation, Eurosia ensures your product is fully compliant with EU requirements. Our expert team handles regulatory submissions and can act as your Marketing Authorization Holder (MAH) — delivering results with speed and precision, without compromising quality.
Navigating EU GMP requirements is critical. We offer streamlined, cost-efficient guidance through GMP readiness, mock audits, and coordination of EU GMP inspections, ensuring your manufacturing site meets the highest quality standards — on time and within budget.
EU GMP Compliance & Audit Preparation
Commercialization & Distribution Support
Eurosia goes beyond authorization — helping you distribute and commercialize your products across Europe. Leveraging our network and regional knowledge, we ensure swift market access and sustainable commercial success at a competitive cost.
With deep regulatory expertise, operational agility, and a commitment to speed, affordability, and compliance, Eurosia Pharmaceutical Limited is your reliable partner for entering and succeeding in the European market.
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