On March 20, the State Administration of Market Regulation issued the revised Measures for the supervision and administration of medical device production and the measures for the supervision and administration of medical device operation, which will come into force on May 1, 2022. China will fully implement the system of medical device registrants and recorders, strengthen supervision and inspection measures, improve supervision and inspection means, and strengthen the punishment of illegal acts. Clarify the responsibilities of both the registrant and the entrusted production enterprise, incorporate the relevant requirements of entrusted production management into the quality management system, and further improveRead More →
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