To ensure the appropriateness and consistency of existing processes, the Annual Product Quality Review is a process required by Pharma GMP.Know more
The Master Batch Record is configurable for any given product and batch size (fixed & variable) by creating reusable templates for every activity of the process.
eLog of CaliberBRM tracks and generates reports for operational and non-operational activities including Area Usage, Equipment Usage, Report Configuration, Checklist Issuance & Execution.
The batch record execution can be automated by online process of CEBR or alternatively, an offline process can be initiated by the print of master batch record.
Through CaliberBRM, users can create and execute QI protocols, having full control over QI tests and test results with sample collection alerts.
The material dispensing and receiving can be performed with or without instrument interface, with label printing functionality and a check for dispense quantity.
All the executed templates will be displayed during batch closure and the user can close the batch at any stage in CaliberBRM. Dossier Request and Dossier Generation facilitates the user to convert executed Batch Manufacturing Record into PDFs if required.
CaliberBRM stands tall on the issues of Data Integrity & ALCOA, complying to all Regulatory requirements, and is a bliss for QA… JB Chemicals