Quality Management Systems ISO 13485 – Virtual

This one-day ISO 13485 workshop covers the requirements of ISO 13485 and its implications within a medical device manufacturing company. PharmOut’s consultants regularly design and write Quality Management Systems for companies, from the smallest to the large blue-chip companies. They have many practical suggestions on how to apply the ISO 13485 standard and with ready access to an ex, TGA inspectors can answer the more difficult questions too.

As the ISO Standard 13485:2016 Medical Devices states:

“All requirements of this International Standard are specific to organizations providing medical devices, regardless of the type or size of the organization.”