Understanding Pharmaceutical Documentation
Documentation is a paper that provides information, especially of an official or legal nature, written report, or record. Documentation is the method of preparing written material which describes the process in terms of specifications.
The Batch Manufacturing Record (BMR) is essential quality and GMP documentation for tracing the complete cycle of a manufacturing batch or lot.
The BMR should be checked before issuance to assure that it is the correct version and a legible, accurate reproduction of the appropriate master production instruction.
Before any processing begins, a check should be performed and recorded to ensure that the equipment and workstation are clear of previous products, documents, or... Continue reading "Pharmaceutical Documentation, GLP Standards, and Packaging" »