The development process of injection drug delivery devices allows us to flexibly reflect product requirements and comply with necessary regulatory and normative requirements. Customers can utilize our years of industry experience and resources in the process of cooperating with us.
Develop injection molded drug delivery devices, combination products, and drug packaging in accordance with regulations such as MDR 2017/745, ISO 13485, ISO 15378, FDA 21 CFR Chapter 820. Our product development process allows us to flexibly reflect product requirements and comply with necessary regulatory and normative requirements. Customers can utilize our years of industry experience and resources in the process of cooperating with us. The products we develop are suitable for the expansion of subsequent production scale, whether it is limited quantities of products that need to be quickly provided for clinical research or large-scale production.
During product development, define the necessary assembly and finishing processes as early as possible. Thoroughly review each process and redevelop as needed. We will work closely with you, our internal experts, and external suppliers to find suitable solutions. Based on this, develop and optimize processes to achieve robust production and quality requirements. We will also analyze possible application processes.