Skip to content

cGMP manufacturing

In cGMP manufacturing, all manufacturers are required to keep Master Batch Records (MBRs) and Batch Production Records (BPRs) in order to comply with FDA regulations.

Master Batch Records, also known as Master Manufacturing Formulas, are general manufacturing instructions. Each unique formulation must have its own MBR and should include:

  • Identification of product name.
  • Bill of Materials detailing each component’s weight, measure, or count needed to manufacture the batch.
  • Equipment list.
  • Component list.
  • Statement of theoretical yield at each step in the manufacturing process.
  • Expected yield of the finished product.
  • Specific instructions for each state in the manufacturing process.
  • Sampling and testing procedures.
  • Instructions for manual operations.

The purpose of an MBR is to ensure that all proper ingredients are added and that each step in the process is completed.

What are Batch Production Records?

Batch Production Records are copies of the Master Batch Record. The BPR documents the when, how, by whom, with what tools, and in what environment a product was produced. The Batch Record is where operators record specific lot numbers and the specific weights, measures, or counts of ingredients and components used to produce that specific batch.

While the Master Batch Record serves as a template for the manufacturing process, the purpose of a BPR is to show that each specific batch of product was created in accordance with the MBR and also explain all deviations that may have occurred during the production of any given batch. The Batch Record serves as a controlled record of the process in order to maintain the traceability of raw ingredients and manufacturing practices.

For more information about Batch Production Records and their work in InstantGMP™, click here.


Back To Top