The Approved Suppliers Register is compliant with different quality management standards and can be customised to work within all organisations. If implementing one of the ISO standards such as ISO 9001, an approved supplier’s register is key to ensuring only adequate suppliers and contractors are used.
The Calibration and Maintenance Register is important for different ISO standards such as ISO 9001, ISO 14001, ISO 45001 and ISO 27001 amongst other. This register helps an organisation to stay on top of necessary calibration and maintenance.
The Change Management Procedure is key to managing any change within an organisation, as well ensuring an assessment of its impact and associated risks is carried out.
The Change Request Form is an efficient tool to record a change within operations, as well as carry out an assessment of its impact and associated risks.
The Contractor Performance Review is compliant with different standards, including but not limited to ISO 9001, ISO 14001, ISO 27001 and ISO 45001. The performance review can be adjusted further to meet the organisations special requirements.
The Design and Development Procedure is one of yje key procedures within a Quality Management System (QMS). This procedure will help you to plan your design and development needs.
The Document Control Procedure is used to define how documents are controlled within an organisation, including naming methodology, review and approval.
The Document Register is used as one of the tools to manage documentation and provide an overview of all controlled documents and their revision number.
The Document Retention Policy is compliant with all of the most popular ISO standards related to quality, environmental, information security and health & safety management system. The policy can be customised to work with any organisation.
We use cookies to ensure that we give you the best experience on our website. If you continue to use this site we will assume that you are happy with it.Ok