As a professional GMP manufacturer of steroidal and peptide pharmaceuticals, we are dedicated to providing outstanding global distribution services for a comprehensive range of products, including Active Pharmaceutical Ingredients (APIs), Finished Dosage Forms (FDFs), and CDMO solutions.
Our founding team possesses over a decade of industry experience, having successfully expanded into markets across Europe, the USA, and Australia, which has earned us a strong reputation and deep international expertise. We have established stable, long-term partnerships with many of the world's leading steroidal and peptide brands and remain committed to continuously strengthening these strategic relationships.
Superpharma Group specializes in the production of steroidal and niche non-steroidal APIs. We also provide custom manufacturing solutions tailored to meet the specific needs of our clients. Currently, we operate 2 R&D centers and 2 manufacturing sites. Both sites have successfully passed inspections and audits by leading global pharmaceutical companies, including Novartis, as well as major European partners such as Sanofi and Roche.
As a certified GMP and FDA-inspected facility, we maintain rigorous production and quality systems dedicated to manufacturing high-purity steroidal and peptide products. Our regulation support extends across the entire drug lifecycle, partnering closely with manufacturers to provide comprehensive compliance services. These include DMF registration and EU‑GMP consultation — covering compilation, submission, deficiency response, gap analysis, and pre‑inspection support — along with lifecycle management such as annual reporting and post‑approval changes.
