NEWS DETAIL

The launch meeting for NÜVE's Product Development Procedure took place on May 18, 2023. The procedure was prepared based on the system engineering approach, best practices, the company's current operations, and the requirements of TS EN ISO 13485 Medical Devices - Quality Management Systems standard.

In the first session of the meeting, attended by NÜVE management and representatives from all departments involved in the product development process, a presentation was given to inform them about the method and content of the "Product Development Procedure" during its creation.

In the second part of the meeting, the representatives from each department provided their feedback on the flowcharts created for each stage of the product development process, including "requirements identification," "concept development," "preliminary design," "detailed design," "prototype production," "verification," and "validation."

We hope that the procedure, updated based on the recorded feedback, will be beneficial for NÜVE. We consider this procedure, which defines the framework, activities, responsibilities, and input-output relations of the product development process, as an important step in NÜVE's corporate transformation journey.

We want to say thank you to the entire NÜVE team for working so hard and collaborating with us during the procedure creation.