NPI is the core enabler for successful product transition from design to mass production.

Through systematic process development and validation workflows, we can significantly shorten time-to-market, reduce development costs, and ensure stability and consistency in product quality. Our experienced NPI team will engages in early-stage design reviews and proactively identify manufacturing risks through DFM analysis.

In high-demand industries such as medical devices, we have an experienced DFM team that enables us to identify potential manufacturing issues early in the design phase. We provide effective solutions through design reviews, tolerance analysis and process evaluation. We focus on DFM and mold design and fabrication to ensure efficient transition from design to mass  production.

We have a complete validation system (IQ/OQ/PQ) and documentation management capabilities to ensure rapid compliance with regulatory audits such as FDA and CE. Additionally, by establishing control limits for key process parameters and contingency plans for supply chain development, we can effectively respond to raw material fluctuations and equipment malfunctions, ensuring continuity in production.