A) assesses ability of personnel to maintain sterility of hands and fingertips during handwashing, garbing, and gloving as well as during sterile compounding B) to eliminate contamination accumulated under the fingernails C) because it is almost impossible to compound without fingertips D) it allows your fingertip to become more susceptible to non-hazardous products
A) 10 B) 3 C) 1 D) none needed
A) true B) false
A) every 6 months immediately after washing, garbing, and gloving B) all the options are correct C) verify validity with external laboratory testing D) three consecutive successful times times prior to authorizing personnel E) immediately after media-fill test
A) label, seal, package, and ship samples, provide all required information, and ship samples as per third party instructions B) review results and ensure CFU counts are within standards C) all options are correct D) ensure external entity providing services has satisfied vendor qualification procedures
A) true B) false
A) no need to worry about positive and negative control since they cancel each other out B) all tests can be groupped C) ensure personnel being tested do NOT disinfect gloves before the test
A) false B) true
A) unopened growth media plate B) disinfected vial C) both opened and/or unopened D) opened growth media plate
A) right before hand washing, garbing, and gloving B) during hand washing, garbing, and gloving C) all options are correct D) immediately following hand washing, garbing, and gloving |