Appeal to manufacturers: take action to meet IVDR requirements
The Dutch Health and Youth Care Inspectorate (IGJ) has conducted a survey of Netherlands-based manufacturers of medical devices for in vitro diagnostics (IVDs). The IGJ wished to gain insight into how the transition to the European regulation on medical devices for in-vitro diagnostics (IVDR) is progressing. This publication describes the results of the survey.
Based on the outcome of the survey the IGJ appeals to manufacturers to meet the IVDR requirements before the deadline.