ISO 18788 provides a framework for establishing, implementing, operating, monitoring, reviewing, maintaining, and improving the management of security operations. It provides the principles and requirements for a security operations management system (SOMS).
ISO 18788 provides a business and risk management framework for organizations conducting or contracting security operations and related activities and functions while demonstrating:
This globally recognized Information Technology Service Management Standard was inspired by the British Standard BS 15000 model and aligned with the process approach defined by the Office of Government Commerce (OGC)’s IT Infrastructure Library (ITIL). ISO 20000 has been designed to shape consistency in the management of IT services and infrastructure, either internal or outsourced, benefiting employees and clients.
Competence in any field is crucial, but it’s even more pertinent in the medical sphere where the patient’s system is compromised by disease or injury. ISO 15189 is a mark of confidence awarded to medical laboratories – an accreditation that proves you are dedicated to delivering a proficient and quality service across all aspects of your operation.
Hazard Analysis Critical Control Points (HACCP) is defined to be the food detrimental elements major control points by the food and drug administrative agent. HACCP is composed as hazard analysis (HA) and critical control points (CCP). HA is to search for the hazard elements and analyze the hazard structure. HACCP is to decide the sanitation control points to control the major hazard control points after identifying the hazard elements from material supply, manufacture, processing, preservation and distribution to the end user consumption.
ISO 13485 is an international standard that defines quality management system requirements for manufacturers of medical devices. ISO 13485 contains requirements essential for organizations operating at any tier in the medical devices and pharmaceutical supply chain. The primary objective of the standard is to facilitate harmonized medical device regulatory requirements and as a result, it includes some particular requirements for manufacture, installation, and servicing such as added requirements on record-control, sterilization, and risk management.
AS9100 (BS EN 9100) is the single common quality management standard for the aerospace industry. It is used and supported by the world's leading aerospace companies and throughout their supply chains. AS9100 can be used by organizations across the aerospace sector, including design, manufacturing, maintenance and distributing companies. If you certify to the standard you can be confident that you have an effective quality management system in place. AS9100 may also be essential to achieving your trade license, making it essential now and in the future.
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