Molecular Devices SoftMax Pro GxP

Become 21 CFR Part 11 compliant for microplate readers     

SoftMax® Pro 7.1 GxP Software is the latest, most secure software to achieve full FDA 21 CFR Part 11 compliance with streamlined workflows to ensure data integrity. Every step is optimized to simplify analysis and reporting to support our microplate readers.           

Our expert team will partner with you to set up single- or enterprise-level software, and provide IQOQ services using our validation package to establish full compliance on your microplate readers. Major data privacy and security improvements support the latest GDPR regulations.           

Windows Active Directory

User administration in a Windows Active Directory or via the GxP Admin software simplifies defining password criteria, reset and change periods, and reduces the amount of IT support.           

Improved signing process     

Users can only sign a single pre- and post-release statement per document contributing to data integrity.           

Roles and permissions  

Permissions are defined on a per role basis and assigned accordingly to users within projects to maintain a structured system. Three predefined roles—Scientist, Lab Manager, Lab Technician—accommodate the document release workflow, allowing first-time users to get started quickly.           

Improved auto-save functionality    

New documents must be saved before they can be modified and documents are automatically saved before and after a read to prevent the loss of data.           

Projects feature     

Project teams can be created where users can be assigned to different projects with different roles but can't have different roles in the same project.           

Auto-export function   

Data can be exported to a location outside the database and various file formats are available to support the import into other applications such as LIMS (Laboratory Information Management System) or SDMS (Scientific Data Management System). XML is supported for data export and auto export.