Y
Yano4ka
Dear colleagues!
I have started some months ago in the Quality role in a medical device company. All improvements that were made so far within the CAPA process. Now I plan for major change in the companies Document Control systems. As far as I understood, I will need to create a quality plan: integrating all aspects in one.
Can anyone help with an example (template to document my activities) or advice where to start from? Shall this processes be part of Risk Management?
Thanks in advance!
Y
I have started some months ago in the Quality role in a medical device company. All improvements that were made so far within the CAPA process. Now I plan for major change in the companies Document Control systems. As far as I understood, I will need to create a quality plan: integrating all aspects in one.
Can anyone help with an example (template to document my activities) or advice where to start from? Shall this processes be part of Risk Management?
Thanks in advance!
Y