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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.

The Master Formula Record should include: the name of the product, with a product reference code relating to its specification; a description of the dosage form, strength of the product. batch size. Shelf Life. Storage Condition.

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.

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 .

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.