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Calibration Management Software for Pharmaceuticals

 

 

Please find below our listing of possible software solutions for the Pharmaceutical, Medical Device or Life Sciences Industry wishing to comply with the FDA, TGA, MHRA regulations.

 

Calibration is the act of checking or adjusting (by comparison with a national reference standard) the accuracy of a measuring instrument or device. Calibration Management software is specifically (usually) designed to manage these activities.

 

The International Society of Pharmaceutical Engineers have an excellent publication covering this critical activity.

 

 

Calibration Management Software:

 

Vendor Claim Website
MasterControl™MasterControl™ integrated QUALITY and COMPLIANCE management software systems for FDA and ISO regulated industries. Integrated software systems include CAPA, Document Control, Training Management / Tracking, Change Control, Audits, Complaints Handling, eProcess Automation, Sarbanes-Oxley (SOX), etc. www.mastercontrol.com
Calibration ManagerCalibration Manager® software, is among the world's leading calibration management database programs. Calibration Manager automatically calculates due dates, tracks histories and prints reports of calibration schedules. It also tracks preventive maintenance. Flexible data retrieval and reporting capabilities permit customization according to your exact needs. The electronic signature functionality was designed to meet FDA 21CFR Part 11 requirements. www.coolblue.com
QSI System, Designed specifically to meet the requirements of ISO 9001:2000, the QSi System for Quality Management helps your organization reap the benefits of ISO certification, including improved customer satisfaction and reduced costs. www.qualitysys.com

 

The above table lists all the Software identified by PharmOut Information Technology.

 

If you are experienced in using one of the software packages listed below and would like to rate the product while sharing your comments and experiences with other visitors, please submit a comments form at the base of this page.

 

If you are a Pharmaceutical, Medical Device, Clinical or Quality Management Systems and Software manufacturer and feel that the details provided are inaccurate, please click here. Alternatively, if you wish to add your software and provided that it is genuinely designed to meet the Life Science Industry regulatory requirements, why not click here!

 

The comments in this site are human verified but not modified, if you leave a legitimate email address and your comments, if relevant to our readers it will be included in the site.

 

 

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