Примери за използване на Validated aseptic на Английски и техните преводи на Български
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Medicine
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Colloquial
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Official
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Ecclesiastic
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Ecclesiastic
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Computer
Validated aseptic conditions.
Controlled and validated aseptic conditions.
At 2-8°C, unless dilution has taken place in controlled and validated aseptic.
In controlled and validated aseptic conditions.
At 2-8°C, unless dilution has taken place in controlled and validated aseptic.
Place in controlled and validated aseptic conditions.
The product is not intended to be stored after dilution unless the dilution has taken place under controlled and validated aseptic conditions.
All steps should be completed under controlled and validated aseptic conditions by adequately trained staff.
The product is not intended to be stored after reconstitution anddilution unless this has taken place under controlled and validated aseptic conditions.
Has taken place in controlled and validated aseptic conditions.
However, due to the importance of microbiological infection risk for injectable products,the reconstituted solution should be used immediately unless reconstitution has taken place in controlled and validated aseptic conditions.
Has taken place in controlled and validated aseptic conditions.
If not used immediately, in-use storage times are the responsibility of the user andwould normally not be longer than 24 hours at 2°C-8°C unless reconstitution/dilution has taken place in controlled and validated aseptic conditions.
Unless this has taken place under controlled and validated aseptic conditions.
From a microbiological point of view, the reconstituted solution should be used immediately,unless reconstitution has taken place in controlled and validated aseptic conditions.
ΟC, unless reconstitution anddilution has taken place in controlled and validated aseptic conditions.
Chemical and physical in-use stability has been demonstrated for up to 24 hours at 2- 8ºC when dilution is performed under controlled and validated aseptic conditions.
If not used immediately,preparation should take place in controlled and validated aseptic conditions.
From a microbiological point of view,the product should be used immediately unless it has been reconstituted under controlled and validated aseptic conditions.
If not used immediately,preparation should take place in controlled and validated aseptic conditions.
Add the content of one ampoule of solvent to one vial containing rasburicase andmix by swirling very gently under controlled and validated aseptic conditions.
If not used immediately, the reconstituted vials can be stored for up to 24 hours at 2°C to 8°C,provided it was reconstituted under controlled and validated aseptic conditions, and must be discarded thereafter.
From a microbiological point of view, the medicinal product should be used immediately unless reconstitution anddilution has taken place in controlled and validated aseptic conditions.
Therefore the reconstituted solution should be diluted under controlled and validated aseptic conditions.
If not used immediately, in-use storage times are the responsibility of the user and would not normally be longer than 24 hours at 2°C- 8°C,unless reconstitution/dilution has taken place in controlled and validated aseptic conditions.
If not used immediately, in-use storage times and conditions prior to use are the responsibility of the user andwould normally not be longer than 24 hours at 2 to 8°C when reconstitution has taken place in controlled and validated aseptic conditions.
If not used immediately, in-use storage times and conditions prior to use are the responsibility of the user and would normally not be longer than 24 hours at room temperature,unless reconstitution/dilution has taken place in controlled and validated aseptic conditions.
If not used immediately, inuse storage times and conditions prior to use are the responsibility of the user and would normally not be longer than 24 hours at room temperature, unless reconstitution(and further dilution, if applicable)has taken place in controlled and validated aseptic conditions.