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ISO 13485:2003 is an international standard that defines quality management system requirements for manufacturers of medical devices.
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ISO 14001 is the internationally recognized standard for managing, mitigating and improving an organization's environmental impacts...
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ISO 28000 is an international supply chain management standard that provides a valuable framework to help minimize the risk of security incidents, helping to provide problem free 'just in time' delivery of goods and supplies...
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ISO 9001 has become the preferred international solution for improving overall organizational performance, achieving customer satisfaction, and promoting continual improvement...
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ISO/IEC 27001 is an international standard that aims to ensure adequate controls are in place to address confidentiality, integrity and availability of information and safeguard the information of 'interested parties'.
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OHSAS 18001 certification can help an organization identify and manage uncontrolled and unnecessary health & safety risks, better safeguarding employees and business...
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Canadian Medical Device Regulations require manufacturers selling class II, III and IV medical devices within Canada to be registered to ISO 13485:2003 by a quality system registrar accredited by the Standards Council of Canada (SCC) and recognized by Health Canada under the CMDCAS program...
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The 98/79/EC Directive helps manage the safe manufacture of in vitro diagnostic medical devices...
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The 93/42/EEC Directive covers all products which claim to have a medical purpose and which are used in and on the human body, from heart valves to scalpels, excluding in vitro diagnostics, which are covered in a separate directive.
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Integrated Management Systems certification can apply to businesses who have a single management system that complies with the requirements of two or more standards...