Teku can coordinate required Validation activities, including Design, Process, Shelf Life, Packaging, Software, Sterilization, and Biocompatibility tests.
Teku will prepare and conduct risk analysis, FMEA, and design reviews, freeing your staff from time-consuming project tasks.
During the entire development process, Teku will maintain Design History documentation in accordance with your company's specifications.
We can work with your Operations staff to ensure smooth design transfer to manufacturing and will continue to support the product to ensure your customers' satisfaction.
Upon approval of intital designs, we will produce prototypes for the team's review. Following team input, further iterations and testing will be conducted until the design is ready to be frozen.
Teku can develop or assist with Device Master Record documentation, such as component/assembly drawings, quality instructions, manufacturing procedures, travelers, and test protocols and reports.
Teku has the ability to integrate closely with your project team to determine how best to satisfy your product design needs. We will work with your Engineering staff to develop Product Specifications and produce initial prototype designs and solid CAD models.
The thorough documentation we provide will minimize further iterations, saving you valuable time in the development process.