Pharmaceutical industries are involved in the manufacturing of medicinal products which are finally utilized by the patients so a great level of care & compliance is required at each level of manufacturing.ĭocumentation in the pharma industry is very important & is also a requirement of various guidelines & regulatory bodies like GMP & US-FDA.ĭifferent types of documentation are carried out in pharmaceutical industries in different departments according to the requirement & BMR or Batch Manufacturing Record is one of the most important documents of the production area. Ensure the Sieve/Screen is used as per mention in the batch record. Check the Line clearance is verified by QA. Ensure the ‘Environmental Condition Log’ is written as per Instruction given in BMR. A batch manufacturing record (BMR) is an important document for chemical and process manufacturers: It tells users how to produce a batch of a given product, then records the entire production process, from start to finish.Įnsure the ‘Weight Verification’ of all ‘Dispensed Materials’ is completed and signed prior to manufacturing.
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