Manufacturers must comply with many standards and legal regulations. In Europe, the Medical Device Regulation (MDR) is of central importance. It stipulates that medical devices must meet the highest safety standards and be comprehensively documented. There are also various QM-relevant standards.
Pramodh Kumar, Project Manager, gives an overview of the standards that are applied in his company, ET Elastomer Technik GmbH: "ISO 9001 ensures global quality management system standards for customer satisfaction. ISO 13485 is essential for maintaining consistent quality in the design, development, and production of medical devices. ISO 14001 focuses on minimizing environmental impact."
Other relevant regulations include ISO 14971, which deals with risk management, as well as specific requirements of the US FDA for market access in the USA.