Shenzhen SafeSecure Medical Infection Control Tech Co., Ltd

(a) According to the requirements of the quality management system, authorize the inspection of the products before release. (b) Responsible for organizing to establish, maintain the latest technical documents and Declaration of conformity and documentation. (c) Responsible for organizing various departments to carry out post market surveillance and alert system event report. (d) Responsible for signing clinical investigation statement.

(a) Responsible for organizing the implementation of product conformity process; (b) Responsible for organizing all departments to compile technical documents; (c) Sign EC-Declaration of Conformity; (d) Responsible for post-marketing surveilliance with another appointment of person responsible for regulatory compliance. (e) Responsible for the promotion and training of laws and regulations in the company.