What is the difference between Statutory Requirements and Regulatory Requirements?The term “statutory and regulatory requirements” appear in ISO 9001:2015 for 12 times. These two requirements together are also called as the legal requirements. However, the question here is: “What is the difference between statutory and regulatory requirements?”. The difference between statutory and regulatory requirements is a subtle
What is the Difference Between an Audit Finding and a Nonconformance? What is an audit?A quality audit is a systematic examination of the processes and procedures in place at a company to ensure that they are all operating as expected.Quality audits are an integral part of any business. They help in identifying areas that need improvement
Before the release of ISO 9001:2015, there used to be two terms in ISO 9001: Documents and Records.Documents describe what needs to be done, and this includes quality manual, procedures, work instructions etc. Documents get changed or revised with time.Records are evidence of work been done. Records can not be changed (generally) and are retained.In
An international standard is a set of requirements and specifications that is recognized by multiple countries and industries. The ISO provides the framework for the establishment, development, management and application of worldwide industrial and commercial standards. These can be used by manufacturers to ensure they produce parts or items that will work in different markets
Benefits to CompanyImplementing a Quality Management System based on ISO 9001 makes it easier to understand and satisfy customer needs.Better management controls and reporting leading meeting the planned Quality Objectives and better customer satisfactionThe continual improvement requirements of the standard require organizations to improve their products and processesImplementing a process approach leads to fewer problems
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