Pangea is a company that provides multiple commercial services focused in the pharmaceutical sector. We have resources to provide service solutions in a number of areas and is committed in providing successful pharmaceutical solutions and implementation for our partners.

Development and Manufacturing Capabilities 

US based Prescription / .OTC pharmaceutical development and manufacturing operation that is registered and inspected by the United States Food and Drug Administration (FDA) and Drug Enforcement Administration (DEA) for cGMP compliance.

Our current drug development manufacturing capabilities include sterile prescription and OTC Products across a variety of dosage forms: 

• Injectables (1mL to 100mL fill)
• Ophthalmic Solutions
• Ointments
• Otic preparations

Our strategic partnerships allow us to develop niche or hard to develop API’s that can fulfill a market need.

Development and manufacturing is our foundation, but we also provide our partners with other additional aspects of drug development and regulatory compliance.

Our Technical and Regulatory Expertise:

FDA regulatory compliance is critical to the development and successful commercialization of pharmaceutical products. Pangea’s technical and regulatory team has years of experience in complex drug development and getting through the FDA approval process. Our partners can rely on Pangea for expert guidance throughout the molecule-to-market process, from beginning to a successful end.