What is EN ISO 13445-3:2019 ?

EN ISO 13408-2:2019 and EN ISO 15763:2019 are both important technical standards that have a significant impact on various industries. EN ISO 13408-2:2019 is a technical standard that focuses on the validation and control of sterile barrier systems used in the production of medicinal products, while EN ISO 15763:2019 is a technical standard that focuses on establishing guidelines for the management of measurement processes in industries.

EN ISO 13408-2:2019 is designed to ensure the integrity and sterility of medicinal products, particularly those that are terminally sterilized. By adhering to the requirements outlined in the standard, pharmaceutical companies can minimize the risk of contamination, maintain product quality, and ensure the safety of patients who rely on their products. The standard provides guidance on various aspects of sterile barrier system design, testing, and monitoring, helping manufacturers implement robust processes and systems that comply with regulatory requirements.

EN ISO 15763:2019 is an essential technical standard that plays a crucial role in ensuring the safety and efficiency of various industries. It aims to ensure that measurements carried out by organizations are accurate, reliable, and traceable, ultimately enhancing product quality and customer satisfaction. This standard provides guidance on implementing effective measurement management systems, addressing key elements such as planning, execution, analysis, documentation, and improvement of measurement processes.

In conclusion, EN ISO 13408-2:2019 and EN ISO 15763:2019 are both important technical standards that have a significant impact on various industries. Adhering to these standards can help ensure the safety and quality of products, improve processes, and enhance customer satisfaction. Compliance with these standards is critical for professionals seeking to comply with international quality requirements and ensure the efficiency and effectiveness of their processes.