Trasis SA | Trasis SA

Trasis offers end-to-end CDMO services, covering the complete development and manufacturing journey from the chemical synthesis of small molecules and peptides to the production of ready-to-use sterile drug solutions.

Early Process Development & Scale-Up

• Scalable API and precursor synthesis, from R&D to commercial production
• Raw material sourcing and cGMP assessment
• Polymorph screening, impurity profiling, and stability studies
• Process analytics and regulatory (CMC) support

Industrialization & Validation

• Analytical standards
• Analytical method development and validation
• Chiral separations and compound purification
• IND and DMF documentation support and submission
• EU QP release support

Intermediate & API Manufacturing

• Preclinical batch production and clinical trial supply
• Industrial-scale manufacturing of APIs, precursors, and intermediates
• Technology transfer and scale-up for commercial production
• GMP and non-GMP manufacturing facilities

Formulation & Sterile Fill & Finish

• Aseptic processing and customized formulations
• Manufacturing of small molecules, peptides, macrocycles, chelators, and inorganic and organic salts
• Cold kits
• Kits for bioconjugation