Ensuring the sterility of medical devices is paramount for patient safety. ISO 11607-2:2019, published by the International Organization for Standardization (ISO), focuses on the crucial validation of processes used to package terminally sterilized medical devices.
What does it do?
Why is it important?
By adhering to ISO 11607-2:2019, manufacturers can demonstrate their commitment to patient safety and the production of high-quality sterile medical devices. This standard plays a vital role in maintaining public trust in the medical device industry.