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Master Formula Record (MFR) is a master document for any pharmaceutical product. MFR contains all information about the manufacturing process for the product. MFR is prepared by the research and development team of the company.

A master batch record (MBR), also known as a master production record (MPR) is a document that contains the approved ingredients, formulation, and instructions guiding the production of a pharmaceutical product.

What is a Master Formulation Record? A Master Formulation Record is used to document the specific information for each individual batch and is an important component of regulatory compliance and effective process control. This detailed record of procedures describes how the drug product is to be prepared.

Master formula record (MFR) is a master document for any pharmaceutical product. It contains all information about the manufacturing process for the product.

The MFR is a set of instructions that tells you how to produce a product batch, while the BMR records what you actually produced. Think of this process like baking a cake: The MFR is your recipe, telling you how much flour to put in, how many eggs to add, how long to cook it for and at what temperature.

The Master Batch Record can be seen as the blueprint of the process, while the Batch Record contains the documentation of one single execution of the process. It explains exactly how a lot of a product is manufactured and provides info on who, when, where and how the different processes steps are executed.

Dosage form name ? Brand name ? Generic name ? Product code ? Label claim of all ingredients ? Product description ? Batch size ? Pack size and packing style ? Shelf life ? Storage conditions ? MFR number and date ? Effective batch number ? Authorization by the production and quality assurance head .