Document and Record Control For Medical Device Quality Management Systems (ISO 13485 QMS)

Описание: It's important to define how you handle your documents and records. Sounds weird, but it's actually quite easy! This is important, because you need these procedures to be compliant with the ISO 13485 which is required for medical device manufacturers.

This is a free video of our Wizard video course which gives you easy-to-follow, step-by-step instructions on how to create your documentation for your medical device. Take a look at our website for more information:
https://openregulatory.com/courses/th...