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After validation of the standards, the method was evaluated in artificially contaminated samples.
However, when the relative concentration of the two analytes in the QC samples was identical to that of the calibration standards, the method performance was acceptable under all three conditions of interconversion.
Without identification and authentic standards, the method was able to estimate the concentration of a virtually unlimited number of compounds thereby providing valuable data to prioritize compounds in risk assessment studies.
Similar(57)
Of the current standard methods, the method suggested by the World Health Organization (WHO) is the prominent.
The difference between the standard method and the new method was less than the difference seen on testing repeatability of the standard method.
Comparison of the standard method and the method modified for infants and young children We compared the standard method and the method modified for infants in 3 healthy adults and 4 CF patients in a preliminary study.
Other non standard sizes: use the standard method mentioned earlier in this article.
By using the standard method, the (PS) condition holds.
With the standard method, the relative error is also very small (0.65%).
The first group used the standard method in the laboratory (U-SQ).
The FPA was evaluated using the standard method of the International Union of Pure and Applied Chemistry IUPACC) [ 36].
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