about us
About
Lokman Hekim
Founded in 2022 in Istanbul, Turkey, Lokman Hekim distills 18 years of cumulative senior-team expertise into a single, fully integrated CDMO. Our strength lies in a multidisciplinary technical core that has already designed, synthesized and formulated molecules now progressing through global clinical pipelines.
about us
We Employ Latest Research Technology & Company
Committed to solving complex challenges, we empower industries with cutting-edge science and engineering for a better, more sustainable future.
Why Choose Lukman Hakim
End-to-End CDMO Solutions
From custom synthesis and formulation to GMP manufacturing and regulatory support, we cover the entire pharmaceutical development cycle under one roof.
Regulatory Excellence
Our QA and regulatory teams include former agency reviewers and QPs, ensuring compliance with FDA, EMA, TGA, and PMDA standards.
Proven Technical Expertise
Multidisciplinary PhD-level chemists, engineers, and pharmacists with 18+ years of experience driving molecules into global clinical
Global Reliability & Value
Competitive pricing, transparent processes, and dependable delivery make us a trusted partner for international pharma companies.
What this means for you
Regulatory & QA Team – Former agency reviewers and QP-designated personnel who ensure every synthesis step, formulation batch and facility qualification meets FDA,