Pharma | Cosmetics | Biotechnology | Veterinary

QSBatch is a development originally designed to historize information in pharmaceutical industry. It allows to create complete electronic records of each batch produced without the cost and complexity often associated with EBR systems. It has proven to be a useful tool for generating reports, analysis and process validation.

QSBatch is a complementary software to automation systems, Scada packages and process historians. The costs of its configuration, start-up and report maintenance are considerably lower than the Reporting tools associated with Scada packages. End users and integrators can quickly implement QSBatch in a wide range of applications.

Applications

  • Electronic Batch Records.
  • CIP/SIP Reporting.
  • Heaters / SAS / Sterilization systems.
  • Periodic Evaluation.
  • Life cycle analysis
  • “Golden Batch” analysis.

Features

  • Compatibility: QSBatch meets industry standard data access protocols that guarantee compatibility with most market Scada packages, HMI, LIMS and MES systems. The software can be easily deployed in existing systems, avoiding expensive technology migrations.
  • All included: QSBatch reports can address virtually all manufacturing activities, including batch publishing, production reports, cycle time analysis, event reporting user activity and periodic evaluation.
  • Easy to configure and use: QSBatch's reporting application is installed on Windows® without license restrictions. Its intuitive menus reduce training costs and encourage the system's use.
  • Data Safeguard: QSBatch stores in SQL database, adding Time-Stamp and security to safeguard the process data integrity in electronic format.
  • Configured, not programmed: Every QSBatch's configuration task is an "easy-click" operation. The reports are generated with less training, lower development costs and fewer mistakes.
  • Regulatory compliance: User security and traceability features of the operations are an integral part of the QSBatch design, which guarantees compliance with CGMP standards and guidelines.