Labelling & Packaging
Medical devices may not change their performance and safety features during transport and storage when complying with the manufacturer's instructions. Therefore the requirements for product packaging must be considered in the development process. In addition to that, the consideration of requirements for product labelling and for instruction for use are important as well.
We would be happy to support you with the implementation of a process for the development of packaging, labelling and instruction for use of your product.
In doing so it shall be ensured that your medical device is functional when the user receives it and subsequently will be able to operate it correctly and safely.