Leveraging our proprietary technology platforms — Phytopower® Development Platform of Bioactive Molecules & Ingredients from Global Medicinal Plants, Aktinsyn® Technology Platform of Synthetic Chemistry, and Aktinbio® Development Platform of Biotechnology, AKTINPHARM® offers integrated CRDMO services to global pharmaceutical enterprises, biotech companies, and Marketing Authorization Holders (MAHs). Our end-to-end capabilities span drug discovery, API process development, CMC studies, formulation development, regulatory documentation support, and commercial manufacturing.
AKTINPHARM® focuses on natural drugs, small-molecule APIs, peptides, ADC linker-payloads, and oligonucleotide drugs/LNP delivery materials. By embedding rapid early-stage R&D, robust process development, in-depth quality studies, and seamless regulatory compliance throughout the entire product lifecycle, we empower our clients to accelerate their transformation from proof-of-concept to IND/IMPD filings and from clinical supplies to commercial manufacturing.
AKTINPHARM® integrates discovery, process development, analytics, formulation development, regulatory support, and manufacturing into a unified technological pipeline for synchronized advancement. Through flexible FTE and FFS collaboration models, we support full-scale development needs ranging from non-GMP R&D samples to GMP clinical and commercial supply, as well as from lab-scale and pilot-scale up to commercial manufacturing, catering to our clients' differentiated demands for speed, cost and regulatory compliance at varying stages.
AKTINPHARM® CRDMO: Making Complex Molecules More Developable, Making Advanced Therapies More Manufacturable.
AKTINPHARM® Pharmaceutical
Product Center
AKTINPHARM® Pharmaceutical Solutions
Drug Research & Development
Drug Discovery
Natural Compounds & Synthetic Chemistry & Custom synthesis services & Target compound screening & Lead Compound Optimization
Quality Research & Analysis Services
Based on the expertise of our analytical research and development, QC and QA teams, we provide quality research and stability study services for active pharmaceutical ingredients (APIs), formulations, intermediates, and registered raw materials that meet regulatory submission requirements.
APIs CRDMO
We provide process route design, development and optimization for innovative and generic drugs, and provide professional services in quality research, process validation, product life cycle management and process safety assessment based on the QbD concept.
Drug Development CRDMO
Based on the formulation process development and production technology platform, and in collaboration with CDMO for APIs, we build an efficient formulation service platform, including the whole process service from pre-prescription to commercial of formulation development and production.
CRDMO for ADC drugs
Aktin Chemicals, Inc. offer comprehensive ADC drug R&D and manufacturing services (CRDMO) spanning early clinical stages to commercial manufacturing, supporting a wide range of conjugated drug modalities (XDCs), including antibody-drug conjugates (ADCs), peptide-drug conjugates (PDCs), and other innovative bioconjugates.
Registration and Application Services
We have a dedicated drug regulatory team that offers clients services for clinical trial applications (IND/CTA) at different stages (P1, P2, P3), new drug marketing authorization applications (NDA/MAA), generic drug marketing authorization applications (ANDA), and product marketing maintenance, including services for product changes, annual reports, and re-registration.