CDMO Contract Development & Manufacturing

TUP’s CDMO services cover full-cycle collaboration from product concept, Design for Manufacturing (DFM) analysis, mold design, trial validation, to mass production and shipment. We are not just a manufacturer, but also a development partner for medical brands — transforming your concepts into scalable, validated, and mass-producible precision medical components.

1Design for Manufacturing (DFM)

Our professional team leads the Design for Manufacturing analysis, assisting customers in optimizing wall thickness, demolding angle, runner and cooling design before mold opening, reducing later mold repair costs and mass production risks.

2Mold Development & Trial Validation

Our in-house mold facility provides rapid trial molding capabilities from sketches to finished products. Combined with Moldflow analysis to predict injection behavior, small-batch trial molding is used to validate dimensions, appearance, and mechanical functions.

3Cleanroom Mass Production & Shipment

Mass production is carried out in ISO Class 7 / 8 cleanrooms, fully compliant with ISO 13485 medical device quality management standards, with support for production validation documents such as PPAP / IQ-OQ-PQ.