ISO 134852016 Medical Devices
What is ISO 13485:2016 Medical Devices?
#ISO13485:2016 is an international standard that specifies requirements for a quality management system (#QMS) for organizations involved in the design, development, production, installation, and servicing of #medicaldevices. This standard is specifically tailored to the medical device industry and is essential for ensuring the safety and effectiveness of medical devices.
Key features of ISO 13485:2016 include:
• Quality Management System:
• Regulatory Compliance:
• Risk Management:
• Product Life Cycle:
• Documentation and Record-Keeping:
• Continuous Improvement:
• Customer Focus:
Read More: https://tuvat.asia/iso-13485-2016-medical-devices/
Follow US: https://www.linkedin.com/company/tuvaustriabic/
#ISO13485:2016 is an international standard that specifies requirements for a quality management system (#QMS) for organizations involved in the design, development, production, installation, and servicing of #medicaldevices. This standard is specifically tailored to the medical device industry and is essential for ensuring the safety and effectiveness of medical devices.
Key features of ISO 13485:2016 include:
• Quality Management System:
• Regulatory Compliance:
• Risk Management:
• Product Life Cycle:
• Documentation and Record-Keeping:
• Continuous Improvement:
• Customer Focus:
Read More: https://tuvat.asia/iso-13485-2016-medical-devices/
Follow US: https://www.linkedin.com/company/tuvaustriabic/
Category
🎥
Short film