Who requires ISO 13485?
A great quality management system is a group of policies and methods which will help assist an organization to match the demands of stakeholders. In some countries of the European Union and Canada, it’s a legal obligation to have quality management in the case of the manufacturing of medical devices.
Moreover, if companies are supplying raw materials or provide services which are related to the medical devices installation, labeling, and technical publication, ISO 13485 certification will also need greatly. However, ISO 13485 is not called a legal requirement for the companies that display an efficient quality management policy, but companies should certify their medical devices with ISO 13485.
GQS Singapore provides certification services for medical devices to ensure its standards according to the requirement of the market.
We at GQS focus on ISO 13485 Certification, ISO 13485 Consultant, ISO 13485 Consultancy services in the Manila, Calamba, Laguna Philippines, Cambodia, Vietnam, Thailand, Indonesia, Malaysia, Brunei, Singapore, and Bhutan.
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