The new partnership starts with clinical needs and uses joint review and milestone management to advance OEM projects. Both parties will establish clear consensus outputs at each stage, from needs clarification, risk assessment, sample validation to mass production implementation, including interface design, material compatibility, and process windows. In terms of design transfer, we establish standardized documentation and a testing matrix to ensure performance consistency from laboratory samples to mass production versions. Through small-batch pilot production and process capability analysis, we gradually solidify key parameters and form a replicable manufacturing solution. Quality and compliance will be pursued in tandem, covering regulatory review, traceability establishment, and change control to ensure the project's robust implementation under varying market access requirements. To accelerate delivery, we employ a rolling schedule and parallel verification strategy, shortening the overall cycle without compromising quality standards. Both parties will regularly review project data and continuously improve reliability and user experience to achieve greater stability and manufacturing efficiency. This collaboration will help us serve more customized needs in a more open and reusable manner.