TQSoft Thermal Validation Software by TQSolutions
EN554, EN285, EN15883, HTM2010, HTM2030, 21CFRpart11, AMS2750D

Products & Services

Our quality control standards are GAMP4 compliant and our TQSoft package has a complete Validation document option plus IQ/OQ options. Our reputation for quality support of our software and hardware options is second to none. Our goal is always to deliver assurance and peace of mind. Your satisfaction is of paramount importance. Several large pharmaceutical customers have audited our equipment and our QA system and FDA accepts validation data from TQS systems.

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TQSoft

• Go to TQSoft page for a full outline of software functionality.
• Data acquisition software for use with a large selection of the leading data acquisition manufacturers. See Specifications for more details.
• Meet EN554, EN285, EN15883, HTM2010, HTM2030 testing and documentation requirements.
• Fully automatic thermocouple calibration with drivers for a wide variety of calibration equipment from leading manufacturers. See Specifications for more details.
• 21CFRpart11 compliant. Please contact us for our compliance summary document.
• An application designed specifically for testing and validation of thermal sterile and disinfectant processes. TQSoft has many additional features that normal data acquisition software simply does not have.
• Machine database
• Operator access profiles.
• Automatically managed Calibration and Calibration Check Reports.
• Test specifications.
• Lethality analysis options.
• Calculations on each scan.
• Calculations on selectable groups on selectable intervals.
• Test ‘stage’ line manual or automatic insert.
• Fully configurable charts.
• Fully configurable data Lists.
• Test data history, management and archiving.
• Merge data from different loggers/tests in secure environment.
• TQS Continuous Automatic Monitoring package can be added to existing sterile or disinfectant machines that have chart recorders installed.
• TQS can be purchased for straight data acquisition without automatic calibration or 21CFRpart11 compliance.
   

SVReports

• Meet EN554, EN285, EN15883, HTM2010, HTM2030 documentation requirements.
• Supplied with huge library of report templates for all processes (see specifications).
• Reports can be tailored to the needs of individual organizations, processes and equipment.
• Exactly replicate existing S.O.P. formats.
• Reports are of presentation quality, instantly produced, easily managed and secure.
• Reports can include graphics, complex calculations based on acquired test data, lethality formulae, and engineering lookup tables. The calculations and lookup tables are validatable.
• Designer & editor  - no need for word processors - work in any language!
• Compress, email, archive with complete Report management tools.
• Convert entire reports into PDF documents for easy transfer, signing, management

TQS System Packages

• Click here for packages

TQS Validation Binder plus IQ/OQ Protocols

• Full support for system validation:
• Quality Documents.
• Functional Specifications.
• Acceptance Tests.
• Upgrade Folder and Support.
• Validation Summary.
• Issues, Resolutions.
• IQ/OQ CD.

TQS Training

• Option for Configuration/Installation Services.
• Introductory Training.
• Refresher Courses.

PDF Manager (Universal Report Manager).

• Innovative solution to convert whole lists of reports into single secue PDF document for distribution, or archiving.