A laboratory water system that can deliver GMP compliance
ELGA's latest whitepaper details the seriousness of non-compliance in pharmaceutical production and how you can ensure you are compliant in all areas. 'On average 4,500 drugs and devices are pulled from U.S shelves each year' due to the FDA 483 form.
The whitepaper contains:
An introduction to form FDA 483 and why they get issued
What happens after a FDA 483 is issued
How the recalls are classified
Water purification for QC success
This whitepaper gives you the knowledge and understanding to work towards acheiving compliance in your laboratory.
