ISO 18113-1:2022-In vitro diagnostic medical devices
What is ISO 18113-1:2022-In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements? ISO 18113-1:2022 specifies the terms, definitions, and general requirements for the labeling of in vitro diagnostic medical devices. Here are some key aspects covered in ISO 18113-1:2022: Scope: The standard applies to […]