LiberoAssurance Training Centre has now published
ISO 13485:2016 Medical Devices Management Systems e- courses
for Awareness, Internal & Lead Auditor
ISO 13485 is the medical device industry’s most widely used international standard for quality management. This standard focuses on safety; it is an effective solution to meet comprehensive requirements for a Quality Management System in the medical industry.
This standards a special tool for companies active in the design, production, sale, and installation and servicing of medical devices, which ensures that all medical devices meet the proper regulatory compliance laws and customer needs.
Our ISO 13485:2016 (MDQMS) courses cover the key requirements and benefits of Medical Devices Quality Management Systems and offer valuable information on how to apply methods and tools to manage Medical Devices Quality.
Participate in the new LiberoAssurance ISO 13485:2016 e-courses and expand your knowledge through our e Learning Platform:
Learn about the key requirements of ISO 13485 Quality Management Systems for Medical Devices standard with our Awareness e-course.
Expand your ability to effectively conduct internal audits within your company or train your audit team to audit ISO 13485 Quality Management Systems for Medical Devices standard with our ISO 13485:2016 Internal Auditor e-course.
Gain the knowledge and skills to conduct third party audits of Quality Management Systems for Medical Devices with our ISO 13485:2016 Lead Auditor e-course.