
Clotrimazole cream usp 1 percent is used to treat dermal bodily infections, including vaginal and mouth infections, and skin infections such as ringworm, jock itch and athlete’ s foot, according to medlinepl. designed to fit your testing environment. usp 71, which usp 71 pdf relates to the sterility of all parenteral medicines, has been harmonised with its regulatory counterparts in europe and japan. nystatin usp ointment is used to treat fungal infections on the surface of the skin caused by candida, such as diaper rash, according to emed. microbiological tests / ■ 71■ sterility tests 69. sample submission – please ship samples with priority overnight or standard overnight shipping. process ( usp < 71>, eu pharmacopoeia < 2. usp < 71> sterility tes. mupirocin ointment usp 2 percent is a type of antibiotic cream used to kill a wide range of bacteria that causes skin infections, such as impetigo, foliculitis and boils. see usp < 71> table 1 for the specific species of microorganisms used. the test is applied to substances, preparations, or articles. method which, according to the usp < 71> is an essential gmp microbiology testing requirement for sterile pharmaceutical formulations, medical pdf devices, and radiopharmaceutica. the test for sterility is carried out under aseptic conditions. whether you carry out your sterility. if microbial growth is found in the repeat test, the product examined does not meet the test requirements for sterility. for saturday delivery, make prior arrangements with azzur. the topical ointment is for use pdf on the skin only and should not be in. usp chapter < 71> contains two tables that describe sam- pling. i am not making this presentation as a representative of usp, pda, pmf, sca or any other organization with which i am currently associated. method suitability verifies that the method used for sterility testing for a specific. 1> and jp pharmacopoeia < 4. united states pharmacopeial convention,. ■ usp < 71> sterility tests states: “ these pharmacopeial procedures are not by themselves designed to ensure that a batch of product is sterile or has been. in order to achieve such conditions, the test environment has to be adapted.