Microbiology FDA 483 (Eagl e Pharma Outsourcing LLC): Microbiological Contamination Prevention Issues
Your container closure integrity test for *** Injection (USP) ***mg/***ml is inadequate, The test used empty vials instead of fille
Your container closure integrity test for *** Injection (USP) ***mg/***ml is inadequate, The test used empty vials instead of fille
Your container closure integrity test for *** Injection (USP) ***mg/***ml is inadequate, The test used empty vials instead of fille
Product contact equipment including *** stopper drums, *** were sterilized without outer wrapping and transferred from Grade A cart to
Specifically, on 03/06/24, during the production of Gozetotide (Illucix) Cold Kit Lot# K-***, your firm’s Pharmacy Manager was observed blocking
Specifically, on 03/06/24, during the production of Gozetotide (Illucix) Cold Kit Lot# K-***, your firm’s Pharmacy Manager was observed performing
Surface monitoring of the filling and stoppering machine is not performed in a timely manner following the completion of aseptic
On April 29, 2024, *** cleaning wipes packed and ready to be used for *** aseptic cleaning in the Grade
Your firm’s containment control and monitoring programs are inadequate to address the possibility of cross contamination of *** pharmaceutical products
In commercial production, sterile *** API is aseptically filled into canisters, approximately *** batch. *** filling, *** canister is opened
During aseptic filling operations, procedure EP2-PRD-SOP-002, “Personnel Behaviour in Aseptic Area” and line specific intervention procedures were not followed