A wide range of medical devices are being developed to suit a range of uses. These products tend to have short lifecycles because they are often improved and enhanced. In order to rapidly and efficiently develop medical devices, it is crucial to take strategic efforts focusing on laws/regulations and approval/certification applications (pharmaceutical affairs applications) from the initial stages of development. Sumika Chemical Analysis Service provides one-stop services for both testing/analysis and regulation consulting—from the initial research stages to approval/certification applications. We can provide you with the optimal solution at each step of medical device development.