LabVantage Is First to Launch Compliant-Ready LIMS Addressing FDA Draft Guidance on Data Integrity
SOMERSET, N.J.–(BUSINESS WIRE)–LabVantage Solutions, the leading provider of laboratory informatics solutions and services, announces the release of LabVantage 8.3, the newest version of its powerful LIMS software and first GxP-compliant solution for data integrity and auditing, to help drug manufacturers conform to the FDA draft guidance on “Data Integrity and Compliance with CGMP.”
The new Dynamic Auditing feature of the LabVantage LIMS platform ensures that companies are able to meet current and proposed regulatory guidance regarding the management of data in temporary memory. New and emerging data integrity standards put forth by the U.S. Food and Drug Administration (FDA), U.K. Medicines and Healthcare Products Regulatory Agency (MHRA), and World Health Organization (WHO) would require the capture of temporary data in electronic records. The FDA draft guidance states that electronic data that will become part of a permanent CGMP record cannot be stored electronically in temporary memory where it could be subject to manipulation.
LabVantage’s Dynamic Auditing tool helps users maintain a clean and complete, GxP-compliant audit trail based on a full history of analytical testing, including:
“LabVantage is the only LIMS provider in the market today to proactively update our software to offer a solution for data integrity and auditing,” said Ram Velidi, President at LabVantage Solutions. “We continue to deliver on our promise to customers to provide state-of-the-art technology that is second to none and is at the leading edge of laboratory information management solutions and the evolving regulatory landscape.”
New Functionality for ELN/LES
LabVantage has also expanded its inventory of Laboratory Execution System (LES) worksheets. In addition to the existing LES worksheets based on Test Methods, new LES worksheets are now available for: QC Batch Testing, used during the testing of unknown samples; Instrument Certification, used to maintain and calibrate instruments; and Finished Product Sample Testing, which facilitates the review of multiple analytical tests on a single sample.
Another new tool is LabVantage’s Chemical Viewer, which has been added to the Electronic Laboratory Notebook (ELN) and LES. With the Chemical Viewer, users can upload a chemical file to a designated location or copy it into the control system. The viewer offers an editable graphic rendering of the chemical structure defined in the file.
Other new features of LabVantage 8.3 include:
For additional information about LabVantage, visit labvantage.com.
About LabVantage Solutions
LabVantage is a multinational enterprise-software platform provider with over 35 years of experience in laboratory informatics, including laboratory information management systems (LIMS), electronic laboratory notebooks (ELN), and laboratory execution systems (LES). It has ongoing relationships with more than 750 clients in 32 countries working in the life science, pharmaceutical, medical device, biobank, food & beverage, CPG, oil & gas, genetics/diagnostics, and healthcare industries. Headquartered in Somerset, N.J., with 450 employees operating in 12 countries, LabVantage offers a comprehensive portfolio of products and services that enable companies to innovate faster in the R&D cycle, improve manufactured product quality, achieve accurate record-keeping, and comply with regulatory requirements. LabVantage LIMS is highly configurable, purpose-built, and 100% web-based to support hundreds of concurrent users and seamlessly interface with instruments and other enterprise systems. For more information, visit www.labvantage.com