SteelToad ISO Audits

SteelToad’s ISO lead auditors are certified with Exemplar Global. We provide high quality, independent, third-party consulting services for your organization. 

The Quality Management Systems Certification Program from Exemplar Global provides proof of competency to effectively audit QMS and to give assurance that audits will be accepted globally. Built-in liaison with industry representatives in accordance with ISO 19011:2018, Exemplar Global’s Quality Management Systems Certification Program provides Lead Auditors with the proof of their competence to effectively manage quality issues. 

ISO 9001

Obtaining ISO 9001 certification tells customers your organization is committed to enhanced customer satisfaction and to meeting all applicable customer and regulatory requirements, building an organization focused on quality management and fulfilling the needs and expectations of your customers. ISO 9001 is a broad-based Quality Management System (QMS) standard and may be applied to any consulting, manufacturing, or service industry organization. 

ISO 20000 

An ISO 20000 Service Management System (SMS) supports the management of the service lifecycle, including planning, design, transition, delivery, and improvement of a quality product for the customer. Developing a quality SMS informs your customers you have established skills in planning, designing, transiting, delivering, and improving your services to your customers. 

ISO 27001

By obtaining an ISO 27000 certification, you inform your customers you have established a framework for information security, which is placed under management control for sustainable, directed, and continuous improvement. Developing an Information Security Management (IMS) system preserves the confidentiality, integrity, and availability of information by applying a risk management system and gives confidence to customers that your risks are adequately being assessed and managed. 

ISO 13485

ISO 13485 adapts the ISO 9000 process-based model for a regulated medical device manufacturing environment. ISO 13485 is a stand-alone QMS standard, derived from the internationally recognized and accepted ISO 9000 Quality Management standard series. ISO 13485 was written to support medical device manufacturers in designing quality management systems that establish and maintain the effectiveness of their processes. It ensures the consistent design, development, production, installation, and delivery of medical devices that are safe for their intended purpose.