Logbook Management is an essential tool for your Quality Management System and the design of its implementation is crucial for the necessary compliance with Good Manufacturing Practices (GMP). Find out more about it in this article or attend the Sophidis Days, which will take place in Tunisia on the 12th and 13th October, where the Technical Director of RC REDOL, Eng. Ana Gonçalves, will talk about all issues related to GMP compliance.
The Logbook itself is a set of bound and sequentially numbered sheets of paper (data integrity), where primary and secondary data regarding the analysis or the equipment registers are registered. It may be made up of blank sheets or pre-printed sheets with text previously approved by Quality Assurance. On the other hand, the responsibility for its management lies with the Quality Assurance department, but the content of the records is the responsibility of the laboratories or production.
Logbook Management must be planned, executed and reviewed under the supervision of an experienced technician. That’s why, if you plan to implement Good Manufacturing Practices or need to make your current system more compliant, you should rely on RC REDOL’s expertise, which has the experience and know-how to take your Quality System to the next level.
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