What is ISO 13756:2018 ?

ISO 13756:2018 is a technical standard developed by the International Organization for Standardization (ISO) that provides guidance on the design and testing of machinery safety measures intended to protect operators from hazards related to human interaction with machinery. The main purpose of ISO 13732-1:2018 is to ensure the safety of machinery operators by minimizing the risks associated with potential hazards during normal operation, maintenance, repair, and other activities.

ISO 13732-1:2018 focuses on ergonomics, addressing various factors such as operator positioning, visibility, reach distances, physical effort required, and ease of use when interacting with machinery controls and workstations. It is designed to minimize the risks associated with potential hazards during normal operation, maintenance, repair, and other activities of machinery, such as fires, electrical shock, and crushing.

ISO 13732-1:2018 is an essential standard for machinery manufacturers, as it helps them to ensure that their products meet the requirements for safety and usability. It is also important for regulatory authorities, as it provides them with a standardized framework for evaluating the safety and effectiveness of machinery.

ISO 13445:2018 is an important international standard that pertains to the field of quality management systems for medical devices. It is tailored to the medical device industry and provides a systematic framework for ensuring the safety, quality, and regulatory compliance of medical devices.

ISO 13445:2018 plays a vital role in harmonizing regulations and requirements across different countries and regions. By adhering to ISO 13445:2018, medical device manufacturers can demonstrate their commitment to delivering safe and effective products to the market, while complying with legal and regulatory obligations.

In conclusion, ISO 13756:2018 and ISO 13445:2018 are both important international standards that help to ensure the safety and effectiveness of machinery, particularly in the medical device industry. Adhering to these standards is essential for manufacturers to minimize the risks associated with potential hazards during normal operation, maintenance, repair, and other activities, and for regulatory authorities to evaluate the safety and effectiveness of machinery.