How LabHQ LIMS Addresses the Requirements of the FDA 21 CFR Part 11
The FDA’s, Code of Federal Regulations (CFR), 21 CFR part 11, specifically outlines the criteria for electronic records and signatures.
When it comes to remaining compliant with the FDA's 21 CFR part 11, LabHQ LIMS is the perfect solution. Download our document that details the relevant User Requirements and explains how LabHQ facilitates compliance.
