Regulation Support with LabX
- Read Whitepaper
The United States Food and Drug Administration (FDA) and the European Commission have both defined regulations for the conditions under which regulated companies can submit electronic records in lieu of paper documents.
These electronic records can replace paper records for submission, inspection, and for archiving purposes. These regulations define the measures that must be in place to ensure the integrity, trustworthiness and reliability of the electronic records.
This whitepaper from Mettler Toledo gives you an overview how LabX can help you with the compliance.