ISO 13485:2016 – Medical Devices – Quality Management Systems
The international standard will help organizations in demonstrating their potential for medical devices to the world. Companies also become able to show to the customers the regulatory requirements along with the service meeting the customer’s needs consistently. Some organizations are also engaged in one or more platforms of life-cycle. The most vital part for the organizations is the design & development, manufacturing, storage, installation, and servicing of medical devices along with technical support provided for that equipment to the customers.
GQS Singapore always ensures that the international standard must apply by the supplier or outside parties that could clearly disseminate the products with great quality management system-related services to these organizations. We mostly focus on the risk analysis and its management which is clearly linked to the quality system. Hence, this approach will quite different from the usual procedure. ‘GQS Singapore’ helps clients in ISO 13485 Certification, ISO 13485 Consultant, ISO 13485 Consultancy services in the Philippines, Cambodia, Vietnam, Thailand, Indonesia, Malaysia, Brunei, Singapore, and Bhutan. You can send us the email on; [email protected], and we’ll back to you.