CATUG Biotechnology is a technology-driven CRDMO platform supporting nucleic acid and advanced therapeutics from early research to GMP-oriented CMC execution. Built around integrated capabilities in plasmid DNA, RNA drug substance, LNP/tLNP and novel delivery systems, protein/nanobody manufacturing, analytical development, and GMP manufacturing, CATUG helps global innovators translate complex therapeutic concepts into clinical-stage programs. Since its founding in 2021, CATUG has grown into a team of approximately 200 professionals and established R&D and GMP manufacturing capabilities to support complex therapeutic modalities across DNA, RNA, delivery systems, proteins, and advanced CMC workflows. Guided by our core values — Focus, First, Fast, and Flexible — CATUG provides both modular and end-to-end CMC solutions, connecting early innovation with scalable manufacturing, analytical control, quality systems, and regulatory-aligned documentation to accelerate clients’ programs toward clinical development and commercialization readiness.
CATUG has received industry recognition for its RNA-LNP platform capabilities, CDMO execution, advanced therapy enabling infrastructure, and global-quality readiness.
2022
Recognized for CDMO capabilities and execution in the biopharmaceutical industry.
2023
Selected for the KPMG China 2nd Biotech Top 50 List.
2023
CATUG has earned its spot on the list for its exceptional overall strength.
2025
Suzhou CDMO facility successfully passed EU QP audit, strengthening global GMP readiness.
2025
Recognized through project execution supporting China and U.S. IND-stage programs.
Ongoing
Ongoing recognition for integrated RNA-LNP CMC, GMP manufacturing and global project support.
More recognitions and certifications will be continuously added as CATUG expands its global CRDMO platform.