With manufacturing sites approved by the EU and US FDA, Medicamen is well-positioned to serve regulated markets. They serve as the foundation for Medicamen’s expanding role in global product development and innovation.
Strategically located R&D and manufacturing facilities are the backbone of Medicamen’s ability to scale, uphold uncompromising quality, and move with agility across its pharmaceutical business. This integrated footprint positions the Company to meet global demand with speed and confidence, while maintaining the highest standards of safety, precision, and performance.
Our commitment to excellence is validated by globally recognized certifications and regulatory approvals.
World Health Organization Good Manufacturing Practices certification ensuring international quality standards.
International Organization for Standardization quality management system certification.
United States Food and Drug Administration approval for manufacturing and quality systems.
European Union Good Manufacturing Practices certification for export to European markets.
Schedule a facility tour to witness our world-class infrastructure and quality systems firsthand. Discover how we maintain the highest standards in pharmaceutical manufacturing.
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