NSF International Strategic Registrations (NSF-ISR) is a leading global certification body, known for its superior technical expertise and customer satisfaction. Through the highest level of integrity, the NSF-ISR mark is recognized as the gold standard of the certification industry. Whether you are looking at getting certified for the first time or transferring an existing registration, NSF-ISR is here to support you throughout the process with industry recognized leadership and expertise. Use of any NSF International consulting service does not, in any way, make NSF-ISR certification simpler, easier, faster or less expensive. NSF-ISR makes its certification evaluations and decisions impartially and independent from any NSF International activity. Free download apm6852 fridge freezer manual programs that help. Aug 05, 2017 Download Nsf Iso Registration Code. ReadyTalk delivers audio and web conferencing services that inspire collaboration and enable the Future of Work for. Watts Regulator Co., Mueller Steam Specialty Division. 1491 Hwy 20 West. Pauls, North Carolina, 28384, United States has been assessed by NSF-ISR and found to be in conformance to the following standard(s). ISO 9001:2008. Scope of Registration: The design and manufacture of strainers, check valves and butterfly. High temperature bearings and bearing units. SKF high temperature bearings are designed to deliver increased reliability, reduced complexity and decreased. ISO 13485 sets regulatory requirements or, when specified, customer requirements for a management system for medical devices or services. The primary objective of ISO 13485 is to harmonize medical device regulatory requirements for quality management systems. The standard is specific to organizations providing medical devices or services, regardless of the type or size of the organization. Based on the ISO 9001 process approach to quality management, ISO 13485 focuses on what manufacturers must do to provide safe and effective medical devices. Benefits of Certification The benefits of ISO 13485 certification include demonstration of regulatory compliance and more effective risk management. Certification aids compliance to national or international regulatory requirements. Certification also confirms to customers, suppliers and other stakeholders that the organization is in a state of control over its operations. Third-party certification is preferred in many international markets, and is the accepted basis and starting point to achieve the medical device CE mark. It can also be used as a bench mark to meet good manufacturing practice (GMP) compliance in the United States. An ISO 13485 certified quality management system can aid access to U.S. And international markets. Why Work With NSF? Our experienced auditors bring real-world knowledge and practical experience to our auditing program. In addition: • NSF-ISR offers value-added auditing.
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