ISO 50001-2011 Energy Management System
ISO 50001:2011 specifies requirements for establishing, implementing, maintaining and improving an energy management system, whose objective is to enable an organization to follow a organized approach in achieving continual improvement of energy performance, including energy efficiency, energy use and consumption. ISO 50001:2011 specifies requirements applicable to energy use and consumption, including measurement, documentation and reporting, design and procurement practices for equipment, systems, processes and personnel that contribute to energy performance.
ISO 13485:2016 Medical Device
ISO 13485 is an internationally published standard that defines requirements within quality management systems for manufacturers, suppliers, contract service and distributors of medical devices and equipment. The main objective of the standard is to facilitate harmonized quality management system requirements for regulatory purposes within the medical devices sector. ISO 13485 Standard has been based on the requirements of ISO 9001 standard and has the same structure in terms of clauses. Even some clauses of ISO 13485 have been referred to ISO 9001. The ISO 13485 standard is for medical devices – quality management systems – requirements for regulatory purposes, is the basis for regulatory compliance in local and most global markets. Exporting medical Devices to various countries is mandatory. ISO 13485 Certification is an objective evidence of compliance of the requirements
ISO 22301-2012 Business Continuity Management System
ISO 22301 is the Business Continuity Management System standard which with be replacing the BS 25999-2 standard in November 2012. Business Continuity Management (BCM) has been developed to protect companies from the risks associated with company outages which can occur due to unexpected disruptions or disasters.
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