Safety and quality are non-negotiable in the medical devices industry because service lapse could impact human lives. In this regard, ISO 13485 establishes requirements for comprehensive quality management for the design and manufacturing of medical devices. It is a stand-alone QMS standard accepted as for ISO 9000 quality management standard series. It adapts the ISO 9000 process-based model for a regulated medical device manufacturing environment. The standard is more prescriptive in nature and requires a more thoroughly documented quality management system.
ISO 13485 Certification can help an organization improve overall performance, enhance certainty, and expand market opportunities related to its processes and products. Organizations with this certification system demonstrate a commitment to quality for all stakeholders. Some of the benefits foreseen are:
KBS is one of the most trusted brands for management systems certification, including Medical Devices – Quality Management Systems, and can provide ISO 13485:2016 Certification. Since its inception, KBS has certified more than 5000 organizations worldwide including Delhi Metro, Indian Railways, Indian Oil, ONGC, and various other private sector organizations with a diverse scale of operations. With experience in diverse management systems standards, KBS is in a strong position to provide Integrated Management Systems certification to its clients that provides an integrated approach for an organization to adopt Quality, Environment, and Health & safety aspects, amongst others. The auditors and experts at KBS have in-depth knowledge, sharp auditing skills, and proven competence in the field demonstrating utmost sincerity and due professionalism.