Medical Devices Training (ISO 13485)

ISO 13485:2016 is the medical industry's optimal medical device standard, which ensures that all medical devices meet the proper regulatory compliance laws and customer needs. ISO 13485 certification is a valuable credential put in place to keep professionals and customers safe in clinics, hospitals and other medical settings.

ISO 13485:2016 is based on the ISO 9001 process model approach and is a management systems standard specifically developed for the manufacture of medical devices. Its primary objective is to facilitate harmonised medical device regulatory requirements.

Our Medical Devices Quality training courses are designed to help you:

  • Put quality control measures in place

  • Identify and manage risks

  • Comply with relevant legal regulations

  • Manage traceability and recall

  • Improve organisational processes

  • Improve products

  • Increase operational efficiency

NQA is also a proud CQI and IRCA Approved Training Partner, and you can find many CQI and IRCA certified courses within our portfolio.