Overview of the current changes to the Medical Device Regulation (MDR). We collected all helpful data within the ColabON tool. This involved

Product Labeling for Medical Devices is an essential part of the certification process and the technical documentation. It involves process requirements for product development and product requirements. Why is Product Labeling for Medical Devices an important aspect? Product Labeling for Medical Device is a critical aspect of medical device development and regulatory compliance. A clear, accurate, and comprehensive label is essential for: Patient safety:  Ensuring safe use by