Cleaning Critical GMP Areas including Clean rooms
Organizations have to apply well defined GMP practices in Clean rooms and labs in order to maintain particulate and pathogen free environments. There are formal requirements and guidelines for food, drug, medical device and cosmetics manufacturing such that sanitized conditions are maintained. There are several cleaning standards including the ISO14644 and the Federal Standard 209E standards. This can bring up some unique challenges when it comes to tracking assets inside these areas. Since they are operated under strict guidelines, they are subject to several cleaning methodologies. Some of the common SOPs (standard operating procedures) include chemical wipe downs, autoclaving etc. This means the RFID tagged assets in the clean rooms
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