Navigate 21 CFR Part 11 Confidently with Confience LIMS
Laboratory Information Management System (LIMS) software is an essential tool for adhering to Title 21 CFR Part 11 of the Code of Federal Regulations — guidelines set by the U.S. Food and Drug Administration (FDA) concerning electronic records and signatures. As laboratories shift to digital systems for enhanced workflow efficiency, compliance with these regulations becomes of paramount importance. LIMS support the shift from paper to computerized systems by offering a reliable solution that safeguards the integrity, confidentiality, and accuracy of electronic data at every stage of its lifecycle.
