Batch Record Management System

Batch Record Management System module in eQMS Software, intended to maintain the Batch Records preparation, Approval, issuance, recording of Batch manufacturing details, maintenance of the batch data in order to produce quality products as well as to meet cGMP and current Pharma and Biotech industry manufacturing requirements and procedures.

 

     PROCESS FLOW:
  •  Product is registered by defining the stages.
  •  Unique Product is generated by the system after approval.
  •  All BRM Requests are initiated and submitted by uploading the documents
  •  BRM Request is Reviewed/Approved by various people based on requirement defined in BRM Approval Work Flow (like HOD Review, QA Coordinator Review and QA Head Approval).
  •  Unique BRM No. is generated automatically after approval.
  •  BRM Publish Requests are submitted by entering the effective Date.
  • BRM Publish Request is Reviewed/Approved by various people based on requirement defined in BRM Publish Approval Work Flow (like HOD Review, QA Coordinator Review and QA Head Approval).
  • BRM is Effective based on the Effective date after Publish Approval.
  • Approved BRM are requested for BRM Issuance Request by the Manufacturer by requesting the Issue Batch Size
  • BRM Issuance Request is initiated, Reviewed/Approved based on the work Flow.
  • BRM is printed by the Document Controller or Production In-charge based on the Requirement by issuing automatic Unique batch Number for Issuance with auto update of expiry Date.
  • Printed Documents are Issued and Received.
  • BRM Issuance Reprint and Batch Size Correction Can be done.
  • Received BRM Issuance Requests are requested for BRM Return by uploading the document.
  • BRM Return Request is Reviewed/Approved by various people based on requirement defined in BRM Return Approval Work Flow (like HOD Review, QA Coordinator Review and QA Head Approval).
  • BRM Document is Retrieved by the Document Controller
CHALLENGES:

• As the documents are physical and stored physically, there are high chances of losing them.
• In Manual System May the Manufacturer has the latest Approved BRM which effective
• No auto alerts/reminders.
• BRM issuance, print tracking, Retrieval of the issued document are major challenges in manual system.
• Time Consuming for Review and Approval Process and Unique number generation.

BENEFITS:

• Reduce Time Consuming for Review and Approval Process and Unique number generation
• Increase the productivity and decrease the effort required on each product and improves efficiency.
• It is easy to view the Master, Obsolete, Terminated BMR.
• The latest Effective BRM is reflected at Manufacturer.

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