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