Molecular Devices Introduces Enterprise-Level SoftMax Pro 7.1 GxP Software
27 Nov 2018
Molecular Devices has announced the launch of the new SoftMax® Pro 7.1 GxP Software with complete validation tools which achieves full FDA 21 CFR Part 11 compliance in GMP/GLP labs.
Built on its current, industry-leading data acquisition and analysis software, SoftMax Pro 7.1 GxP Software expands its system audit trail functions to include date and time stamps; enables enterprise-level document sharing with Microsoft SQL database; provides complete control over file access permissions; and maintains data integrity with eSignatures and document workflows.
“Being compliant has never been more important to our customers”, said Greg Milosevich, President of Molecular Devices. “We will partner with you to set up single- or enterprise-level software and provide IQOQ services to establish full compliance on your microplate readers. Major data privacy and security improvements support the latest GDPR regulations.”
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SoftMax® Pro Microplate Data Acquisition & Analysis Software
Molecular Devices®SoftMax ® Pro Software is designed to provide the simplicity, flexibility and power required for advanced data analysis. It provides ready-to-run protocols, analysis algorithms, and 21 different curve fit options. Every step has been optimized for data acquired from a Molecular Devices microplate reader or data imported from another source to simplify analysis and reporting. FDA 21 CFR Part 11 compliance tools are available for regulated laboratories providing end-to-end chain of custody.