April 01st, 2019
This guidance outlines the general principles and approaches that FDA considers appropriate elements of process validation for the manufacture of human and animal drug and biological products, including active pharmaceutical ingredients (APIs or drug substances), collectively referred to in this guidance as drugs or products. This guidance incorporates principles and approaches that all manufacturers can use to validate manufacturing processes.
To read the full document go to https://www.fda.gov/downloads/drugs/guidances/ucm070336.pdf
Check out Saint-Gobain Medical Components Process Validation Datasheet at https://www.medical.saint-gobain.com/sites/imdf.medical.com/files/process_validation_datasheet_fls-5296-319-lsmcf.pdf