Registration of regulations: the R & D unit shall divide the regulations in the "Regulations overview table" into quality management system regulations and product regulations. The regulations of quality management system will affect the formulation and content of the company's procedures, and the rules of product law will affect the safety test of medical equipment products of the company. Therefore, the quality management system regulations should be transferred into the "regulations and procedures comparison table" and the product regulations should be filled in the "product safety comparison table". If the regulations are updated, the procedures corresponding to the regulations shall also be updated to ensure the linkage between the regulations and the quality management system.<br>
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