![]() 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. 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. 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. 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. Better compliance with regulatory requirements and ensured customer satisfaction.Improved and stronger decision making based on established facts & figures demonstrated safety of the produced medical devices.Improved company’s reputation as the certified organizations perceived as self-conscious and responsible for the quality of medical devices manufactured for its customers.Organizations with this certification system demonstrate a commitment to quality for all stakeholders. ISO 13485 Certification can help an organization improve overall performance, enhance certainty, and expand market opportunities related to its processes and products. The standard is more prescriptive in nature and requires a more thoroughly documented quality management system. It adapts the ISO 9000 process-based model for a regulated medical device manufacturing environment. It is a stand-alone QMS standard accepted as for ISO 9000 quality management standard series. Global regulatory requirements emphasise this and make it mandatory for such standards. Having a proper QMS in place is essential for medical device-related companies. ![]() In this regard, ISO 13485 establishes requirements for comprehensive quality management for the design and manufacturing of medical devices. The ISO 13485:2016 standard specifies requirements for the Medical Device Development and Quality Management System (QMS) that should be used by medical device-related companies. Safety and quality are non-negotiable in the medical devices industry because service lapse could impact human lives. ![]() ISO 13485:2016 Medical Devices Quality Management Systems ISO 13485 certification is a valuable credential put in place to keep professionals and customers safe in clinics, hospitals and other medical settings. ![]()
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