ISO 22301:2019 Business continuity Management System ISO 22301 certification will help improve the way any business manages this eventuality. It ensures a planned effective business continuity management (BCM) system is in place, enabling you to respond effectively to any disruption. ISO 22301 specifies requirements to plan, establish, implement, operate, monitor, review, maintain and continually improve a documented management system to protect against, reduce the likelihood of occurrence, prepare for, respond to, and recover from disruptive incidents when they arise. Implementing the results of a ISO 22301 certification audit from ABI will increase your organization’s resilience and recovery
ISO 22000:2018 Food Safety Management System ISO 22000 food safety management standards help organizations identify and control food safety hazards, at the same time as working together with other ISO management standards, such as ISO 9001. Applicable to all types of producer, ISO 22000 provides a layer of reassurance within the global food supply chain, helping products cross borders and bringing people food that they can trust. ISO 22000:2018 certification covers all the processes in the food chain that impact the safety of the end product. The standard specifies the requirements for a comprehensive food safety
ISO 14001:2015 (Environmental Management System) “The International Organization for Standardization (ISO) defines an environmental management system as “part of the management system used to manage environmental aspects, fulfill compliance obligations, and address risks and opportunities.” ISO 14001 Environmental Management System (EMS) is a systematic framework to manage the immediate and long term environmental impacts of an organization’s products, services and processes. ISO 14001 helps businesses of all sizes across all sectors make their day to day operations more sustainable. Sustainability can ultimately save money, improve brand reputation, engage employees and build resilience against uncertainty as
ISO 13485:2016 Medical Devices (Quality Management Systems) Requirements for Regulatory Purposes, sets the basis for a quality management system for organizations involved in the life-cycle of a medical device. ISO 13485 is based on ISO 9001 but the requirements are specific to design and manufacturing in medical device industry. ISO 13485 adapts the ISO 9000 process-based model for a regulated medical device manufacturing environment. ISO 13485:2016 certification provides and boosts a confidence and creates a credibility of the organization in the mind of the stakeholder, Directors and clients. An ISO 13485 Certification for Your Business Could
ISO 9001:2015 Quality Management System Supporting an organization’s aims and objectives, an ISO 9001 quality management system (QMS) documents the processes, procedures, and responsibilities for achieving quality policies and objectives. Based on seven quality management principles, the ISO 9001:2015 certification defines the way an organization operates to meet the requirements of its customers and stakeholders ISO 9001 certification will help your organization to develop and improve performance, as well as demonstrate high levels of service quality when bidding for contracts. Implementing a QMS benefits an organization by effectively identifying customers and stakeholders. This outward looking approach