The EU directives for medical devices require that you establish a post market surveillance system for your product.
Nordic Proof can make available test facilities to confirm that the medical device works as intended, and you can receive systematic input about product improvement.
Nordic Proof partners facilitate that KOL’s are involved in designing post market study. A post market study can give valuable data regarding the effectiveness of the product, clinical effect, health economy etc.
A post marked study will also give you insight regarding work flow in the clinic that the use to the product must adapt to.