I got an assignement to rewrite our “purchasing procedure” to include a method of decision making if the materials/equipment bought needs to be validated or not.
To this day we just used common sense but we would like to have added in our procedure because the company is growing, which makes it harder to track everything.
The materials bought are often equipment like particle counters and temperature dataloggers.
As I’m fairly new to the world of GMP I do not know where to start.
Thanks in advance for your input.