Determination of the Mapping Speed Range

For a sodium or potassium hydroxide content in the range of 5 % m/m as sodium hydroxide, the difference between the results of two determinations carried out in parallel on the same sample should not exceed an absolute value of 0 725 %.

- temperature range of the determinations,

The assessment of demand substitution entails a determination of the range of products which are viewed as substitutes by the consumer.

The applicability and accuracy of the different methods used for the determination of the boiling temperature/boiling range are listed in table 1.

The applicability and accuracy of the different methods used for the determination of the melting temperature/melting range are listed in the following table:

For an optimum determination range of 0 to 10 µg/ml of iron, place 0, 2, 4, 6, 8 and 10 ml respectively of working solution (4.5.2) in a series of 100 ml volumetric flasks.

Five methods for the determination of the boiling temperature (boiling range) are based on the measurement of the boiling temperature, two others are based on thermal analysis.

For an optimum determination range of 0 to 5 µg/ml of cobalt, place 0, 0,5, 1, 2, 3, 4 and 5 ml respectively of working solution (4.4.2) in a series of 100 ml volumetric flasks.

For an optimum determination range of 0 to 5 µg/ml of copper, place 0, 0,5, 1, 2, 3, 4 and 5 ml respectively of working solution (4.4.2) in a series of 100 ml volumetric flasks.

For an optimum determination range of 0 to 5 µg/ml of manganese, place 0, 0,5, 1, 2, 3, 4 and 5 ml respectively of working solution (4.4.2) in a series of 100 ml volumetric flasks.

This method allows a determination of whether gases mixed with air at room temperature (circa 20 °C) and atmospheric pressure are flammable and, if so, over what range of concentrations.

It can be assumed for the purpose of the determination of the wholesomeness of foodstuffs treated with an overall average dose of 10 kGy or less that all radiation chemical effects in that particular dose range are proportional to the dose.

temperature range of the determinations,

Determination of the damping characteristics in the resonance range."

BS 4634 Method for the determination of melting point and/or melting range

The limit of determination (1) shall be within the range 1 to 10 mg/kg of dry matter.

The limit of determination (1) shall be within the range 1 to 10 mg/kg of dry matter. 3.

Determination of the suspension characteristics and the range of adjustment to the driver's mass."

Where the active substance is capable of forming ions, determinations must also be made in the acidic range (pH 4 to 6) and in the alkaline range (pH 8 to 10), and be reported.

If there are no suitable data available, a range finding study may be performed to aid the determination of the doses to be used.

This method is suitable for the determination of egg yolk concentration in the range of 40 to 250 g/l in egg liqueur and liqueur with egg.

Chemical products for industrial use - Determination of vapour pressure of solids and liquids within range from 10 1 to 105 Pa - Static method.

These water solubility determinations must be made in the neutral range (i.e. in distilled water in equilibrium with atmospheric carbon dioxide).

Chemical products for industrial use - Determination of vapour pressure of solids and liquids within range from 10 3 to 1 Pa - Vapour pressure balance method.

For an optimum determination range of 0 to 10 mg/ml of iron, place 0, 2, 4, 6, 8 and 10 ml respectively of working solution (4.5.2) in a series of 100 ml volumetric flasks.

For an optimum determination range of 0 to 10 ig/ml of iron, place 0, 2, 4, 6, 8 and 10 ml respectively of working solution (4.5.2) in a series of 100 ml volumetric flasks.

For an optimum determination range of 0 to 5 mg/ml of copper, place 0, 0,5, 1, 2, 3, 4 and 5 ml respectively of working solution (4.4.2) in a series of 100 ml volumetric flasks.

For an optimum determination range of 0 to 5 mg/ml of cobalt, place 0, 0,5, 1, 2, 3, 4 and 5 ml respectively of working solution (4.4.2) in a series of 100 ml volumetric flasks.

Determination of shed antigen in baseline serum samples revealed that 64 % (286/ 447) of patients had detectable shed antigen, which ranged as high as 1880 ng/ ml (median = 11 ng/ ml).

More frequent determinations may be necessary, for example, in patients with renal impairment or with an increased risk of bleeding. – Target range (therapeutic window) for the aPTT:

This method allows a determination of whether gases mixed with air at room temperature (circa 20 C) and atmospheric pressure are flammable and, if so, over what range of concentrations.

For the determination of pure active substance, the calibration range must extend (by at least 20 %) the highest and lowest nominal content of the analyte in relevant analytical solutions.

The limit of determination (1) for HCB shall be within the range 1 to 10 ng/l for waters and 0,5 to 1 mg/l for effluents depending on the number of extraneous substances present in the sample.

The limit of determination (1) for HCBD shall be within the range 1 to 10 ng/l for waters and 0,5 to 1 mg/l for effluents, depending on the number of extraneous substances present in the sample.

This range of possible forms of documentary evidence of origin allows account to be taken of the various degrees of importance of origin determination, having regard to the variety of interests involved.

In a supporting study of ReFacto AF, 1 de novo and 2 recurrent inhibitors (all low-titre, central laboratory determination) were observed in 110 patients; median exposure of 58 ED (range 5-140) and 98 patients had at least 50 ED to ReFacto AF.

If both accuracy and precision are constant over a concentration range around the limit of detection, then the limit of quantification is numerically equal to six times the standard deviation of the means of blank determination (n 20, see 1.2.7).

The method uses defined starting doses and is not intended to allow the calculation of a precise LD50, but does allow for the determination of a range of exposure where lethality is expected, since death of a proportion of the animals is still the major end-point of this test.

When a hydroquinone content considerably higher than 2 % is found and an accurate estimate of the content is required, the sample extract (5.1) should be diluted to a similar concentration as would be obtained from a sample containing 2 % hydroquinone, and the determination repeated. (In some instruments the absorbance may be out of the linear range of the detector for high hydroquinone concentrations.)