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Master formula record (MFR) is a master document for any pharmaceutical product. A MFR should have following parts: Product Details: First on the first page following details about the product are added. Name, logo and address of the manufacturing company. Dosage form name. Brand name. Generic name. Product code.
MASTER FORMULA — A document or set of documents specifying the raw materials with their quantities and the packaging materials, together with a detailed description of the procedures and precautions required to produce a specified quantity of a finished product.
MASTER FORMULA RECORD 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 used as reference standard for preparing batch manufacturing record (BMR) by manufacturing units.
Definition of Master Batch Record Master Batch Record means the document that defines the manufacturing methods, materials, and other procedures, directions and controls associated with the manufacture and testing of the Product, which may be amended in writing from time to time by mutual agreement of the parties.
Batch manufacturing record is a written document of the batch, prepared during pharmaceutical manufacturing process. It contains actual data and step-by-step process for manufacturing each batch. Batch manufacturing record is like a proof that batches were properly made and checked by quality control personnel.
Master Manufacturing Record means, for each Project, the template document proposed by Paragon and approved by Client that defines the final and complete manufacturing methods, test methods, materials, and other procedures, directions and controls associated with the manufacture and testing of Product.
Master Batch Records (Mrs) are general manufacturing instructions. Batch Records are derived from them and refer to a specific order. Master batch records and batch records are therefore the basis for a precise and detailed description of pharmaceutical manufacturing processes.
Batch manufacturing record is a written document of the batch, prepared during pharmaceutical manufacturing process. It contains actual data and step-by-step process for manufacturing each batch. Batch manufacturing record is like a proof that batches were properly made and checked by quality control personnel.
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