We offer an extensive portfolio of 150+ active pharmaceutical ingredients and intermediates, covering multiple therapeutic areas, with more than 30 years of off-patent API manufacturing experience to our pharmaceutical partners.
Curia Generic APIs
Curia offers an extensive portfolio of 150+ generic APIs, covering multiple therapeutic areas. We offer more than 30 years of generic API manufacturing experience to our pharmaceutical partners.
Products with existing patent protection are intended for development use and Regulatory Purposes only, under 35 U.S.C. 271(e)(1) and article 10.6 of the Directive 2001/EC as amended by the Directive 2004/27/EC.
White Paper
Curia's Patented Process for Intermediates Useful for Upadacitinib
Products with existing patent protection are intended for development use and Regulatory Purposes only, under 35 U.S.C. 271(e)(1) and article 10.6 of the Directive 2001/EC as amended by the Directive 2004/27/EC.
White Paper
Curia's Patented Process for Intermediates Useful for Deucravacitinib
Products with existing patent protection are intended for development use and Regulatory Purposes only, under 35 U.S.C. 271(e)(1) and article 10.6 of the Directive 2001/EC as amended by the Directive 2004/27/EC.
White Paper
Curia's Patented Process for Intermediates Useful for Etrasimod Arginine
Products with existing patent protection are intended for development use and Regulatory Purposes only, under 35 U.S.C. 271(e)(1) and article 10.6 of the Directive 2001/EC as amended by the Directive 2004/27/EC.
Global Network
9 Manufacturing sites
Access API capabilities across an established manufacturing network in the United States, Europe and India.
Regulatory Support
550+ Global Regulatory Filings
Leverage an established portfolio of DMFs, CEPs and other regulatory submissions across major global markets.
Expertise
30+ Years of Experience
Draw on longstanding experience in API development and commercial manufacturing.
Worldwide Supply
Reaching 60+ Countries
Delivering APIs to customers in more than 60 countries through an established supply network.
Inspection Track Record
Experience Across Multiple Agencies
Inspection history with the FDA, PMDA, ANVISA and other regulators supports worldwide filing and supply.
APIs across multiple routes of administration
Explore APIs for oral, injectable, ophthalmic, topical and other dosage-form applications.
Built for complex requirements
A specialized offering encompassing sterile, high-potency and controlled-substance APIs.
A catalog that continues to evolve
New products are regularly added to complement the portfolio and respond to changing market needs.
Excipients and Fine Chemicals
Access additional products ranging from pharmaceutical excipients to specialized fine chemicals.