EuroGMP
EuroGMP
Your European Partner for cGMP Compliance, Regulatory Affairs, Technology Transfer & Global Market Access.
Euro GMP is a European pharmaceutical solutions company — not a manufacturer. We are regulatory experts, strategic partners, technology facilitators, licensing specialists, and business development advisors. With our European Headquarters in Malta and Bangladesh Office in Dhaka, we connect pharmaceutical manufacturers, biotechnology companies, and healthcare organizations with international expertise, qualified partner networks, and sustainable growth opportunities.
Euro GMP is a European pharmaceutical solutions company with European Headquarters in Malta and a Bangladesh Office in Dhaka. We help pharmaceutical manufacturers, biotechnology companies, and healthcare organizations achieve regulatory excellence and international growth.
Our team operates as regulatory experts, strategic partners, technology facilitators, licensing specialists, and business development advisors. Through a qualified international partner network, we deliver cGMP compliance, regulatory affairs, licensing, technology transfer, laboratory coordination, and healthcare workforce solutions — without owning or operating manufacturing facilities ourselves.
This collaborative model allows us to remain independent, client-focused, and flexible — connecting the right expertise with the right opportunity, wherever in the world that may be.
Learn More About Us →Strategically located in the heart of Europe for regulatory coordination, strategic partnerships, licensing opportunities, and cross-border business development.
Practical, risk-based support for cGMP, EU GMP, WHO GMP, ISO 9001, ISO 13485, quality systems, and inspection readiness.
Deep understanding of Bangladesh's WHO-recognized pharmaceutical sector, skilled workforce, cost competitiveness, and export growth potential.
As a solutions company — not a manufacturer — we provide independent, client-focused guidance without conflicts of interest.
Access to accredited laboratories, CMOs/CDMOs, technology providers, and regulatory experts across Europe and Asia.
CTD/eCTD dossier coordination, regulatory strategy, gap analysis, and product registration support for international markets.
Licensing-in, licensing-out, portfolio evaluation, and strategic partnership facilitation between European and Asian organizations.
Product, process, and analytical method transfer coordination supported by qualified technical partners.
Partner identification, CMO/CDMO search, market entry strategy, and international business matching.
Collaboration with experienced pharmaceutical quality, regulatory, and commercial professionals who are committed to integrity and long-term value.
Our European Headquarters in Malta serves as the strategic centre for:
Direct coordination with European regulatory landscapes, EU GMP expectations, and international compliance standards for organizations pursuing European market access.
Access to European pharmaceutical companies, technology providers, licensing partners, and business development opportunities through our Malta base.
Facilitating licensing-in and licensing-out opportunities that connect European product portfolios with Bangladeshi and Asian market potential.
Coordinating product, process, and analytical method transfers between European technology providers and Asian manufacturing partners.
Bangladesh has emerged as a significant global pharmaceutical manufacturing hub. For European pharmaceutical companies and investors, it offers:
A growing pool of qualified pharmaceutical scientists, engineers, and quality professionals supporting world-class manufacturing operations.
Bangladesh's pharmaceutical industry is recognized by the World Health Organization, with many manufacturers holding WHO-GMP certification.
Significant cost advantages in manufacturing, labor, and operations compared to European and North American production.
A rapidly expanding export market with Bangladesh pharmaceuticals now reaching 150+ countries across Asia, Africa, and beyond.
Strategic positioning for access to South Asian and ASEAN markets, creating opportunities for European licensors and technology partners.
Whether your organization requires regulatory support, quality system development, technology transfer, licensing solutions, laboratory coordination, or healthcare workforce services, Euro GMP is ready to support your growth.
Let's Build Your Success Together.
