ISO13485: 2016 Internal Auditor Training

Browse times：923     author：admin    time：2019-04-12

The ISO 13485 "Medical Device Quality Management System for Regulatory Requirements" standard is based on the ISO 9001:2008 standard and is applied to independent standards for medical devices, emphasizing the requirements of medical device regulations. The new ISO 13485:2016 standard introduces and reinforces a number of best practices in the medical device industry. According to the ISO official website news, ISO 13485:2016 was officially released on March 1, 2016, which has a significant impact on the quality management of the medical device industry.
This course will thoroughly explain the requirements of the medical device industry certification, so that you can fully grasp the relevant requirements of ISO 13485:2016, effectively carry out internal audit work, improve the quality management level of medical device manufacturers, help enterprises improve their independent research and development capabilities, and improve enterprises. Competitive ability, enhance international competitiveness, and promote standardized management of the medical device industry.

【Return list】