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Data Management
Data management addresses different aspects of data collection, analysis, approval & evaluation, and reporting. Ensuring regulatory compliance and potential efficiency gains are the two main drivers for most software and data management projects at Pharmaceutical companies today. From single workstations to multiple networked instruments, SOTAX software solutions improve your data collection, analysis, approval, and reporting processes - while help your organization to comply with current FDA data integrity guidelines and 21 CFR part 11 regulations on electronic records keeping.
q-doc®
q-doc®
Take control of your data with q-doc® data management software. From single workstations to multiple networked clients, q-doc® connects more than 35 different instrument types including different dissolution testers, physical testing instruments, and standard lab balances for consolidated batch reporting. Ensure 100% compliance, easily record measurement data, and simplify paperless evaluation of all tests performed.
WinSOTAX®plus
WinSOTAX®plus
Dissolution software to manage methods, execute dissolution tests on differently automated platforms and report results in full compliance with 21 CFR part 11 requirements. Analyze UV-Vis results with integrated spectrophotometers and ensure accurate blank & standard handling. WinSOTAX®plus allows operation of Xtend™, CE 7smart, and legacy SOTAX dissolution systems.
MDsoft
MDsoft
Dissolution software to setup, execute, protocol, and report dissolution runs of the fully automated AT MD dissolution platform. Designed for maximum flexibility and 100% data integrity of all steps performed, MDsoft ensures complete protocolling from media preparation to self-cleaning according to pre-programmed washing routines. Fully 21 CFR part 11 compliant and easy to use.
TPWsoft
TPWsoft
User-friendly software package to setup, execute, and control the automated preparation of multiple samples with the TPW workstation. All preparation steps are recorded for full traceability of each sample in compliance with 21 CFR part 11 regulations and FDA data integrity guidelines. Additionally, the software allows seamless data transfer with Waters Empower® for automated creation of HPLC run lists.
APWsoft
APWsoft
The easy-to-use software protocols all preparation steps executed with the fully automated APW workstation. Ideal for users in academia to industry AR&D to the QC lab. Simply setup the required preparation steps for assay & content uniformity testing of up to 300 samples. To avoid manual transcription, APWsoft can automatically create run lists in Waters Empower® for HPLC analysis of prepared samples.
