API Manufacturing

With over 50 years of industry-leading experience, Cayman Pharma operates as a premier global partner for API development. We maintain a rigorous quality system proven through successful regulatory audits by major global health authorities. Our commitment to precision ensures the highest purity for your therapeutic innovations.

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EMA/FDA Certified

Global regulatory compliance with a 50-year track record of excellence.

120 Employees

Dedicated team of scientists and manufacturing specialists.

API & Impurities

Comprehensive manufacturing of complex APIs and reference standards.

Non-infringing

Custom synthetic routes developed for patent freedom and efficiency.

ISO Certifications

Accredited to ISO 9001, 14001, and 45001 standards.

100%

Quality Compliance

Commercial API Production

Our core expertise lies in the specialized synthesis of Prostaglandins. We combine rigorous analytical testing with cGMP-compliant manufacturing to deliver molecules that meet the stringent requirements of modern medicine.

Prostaglandins
Latanoprost (CEP)
Bimatoprost
Latanoprostene Bunod
Tafluprost
Travoprost
Epoprostenol sodium
(+)-Cloprostenol
(±)-Cloprostenol
Cayman Pharma manufacturing facility

Expert Registration Support

Connect with our registration specialists to review detailed DMF filings, stability data, or to arrange technical documentation transfers.

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