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Pharmacy
Extraordinary requirements for this branch are mainly a result of the fact that these measuring devices are used for medicine production. Their quality may affect particular drugs quality and as a result exert an impact on patient’s health. Apart from legal regulations valid for a particular region also pharmacopoeia guidelines are adhered to. Pharmacopoeia are documents binding for a particular continent, e.g. American , Japanese, European, Russian pharmacopoeia, etc. American pharmacopoeia is the one of the greatest priority.
There are two chapters devoted to requirements concerning balances, and . The former one describes specification for repeatability and accuracy, the description is as follows:
Repeatability is satisfactory if two times the standard deviation of the weighed value, divided by the nominal value of the weight used, does not exceed 0.10%. If the standard deviation obtained is less than 0.41d , where d is the scale interval, replace this standard deviation with 0.41d
The accuracy of a balance is satisfactory if its weighing value, when tested with a suitable weight(s), is within 0.10% of the test weight value. A test weight is suitable if it has a mass between 5% and 100% of the balance's capacity
Chapter 1251 is not compulsory, it supplies the reader with explanation and definitions of terms that are pivotal when it comes to electronic weighing equipment:
sensitivity
accuracy
linearity
eccentricity
In order to comply to regulations of pharmacy industry it is necessary to meet chapter 41 requirements, especially those intended for repeatability of indications. As it is commonly know, it is repeatability that decides on measuring accuracy, i.e. balance reliability. For microbalances this parameter is used for MSW determination.
Pharmacy
Extraordinary requirements for this branch are mainly a result of the fact that these measuring devices are used for medicine production. Their quality may affect particular drugs quality and as a result exert an impact on patient’s health. Apart from legal regulations valid for a particular region also pharmacopoeia guidelines are adhered to. Pharmacopoeia are documents binding for a particular continent, e.g. American , Japanese, European, Russian pharmacopoeia, etc. American pharmacopoeia is the one of the greatest priority.
There are two chapters devoted to requirements concerning balances, and . The former one describes specification for repeatability and accuracy, the description is as follows:
Repeatability is satisfactory if two times the standard deviation of the weighed value, divided by the nominal value of the weight used, does not exceed 0.10%. If the standard deviation obtained is less than 0.41d , where d is the scale interval, replace this standard deviation with 0.41d
The accuracy of a balance is satisfactory if its weighing value, when tested with a suitable weight(s), is within 0.10% of the test weight value. A test weight is suitable if it has a mass between 5% and 100% of the balance's capacity
Chapter 1251 is not compulsory, it supplies the reader with explanation and definitions of terms that are pivotal when it comes to electronic weighing equipment:
sensitivity
accuracy
linearity
eccentricity
In order to comply to regulations of pharmacy industry it is necessary to meet chapter 41 requirements, especially those intended for repeatability of indications. As it is commonly know, it is repeatability that decides on measuring accuracy, i.e. balance reliability. For microbalances this parameter is used for MSW determination.
Pharmacy
Extraordinary requirements for this branch are mainly a result of the fact that these measuring devices are used for medicine production. Their quality may affect particular drugs quality and as a result exert an impact on patient’s health. Apart from legal regulations valid for a particular region also pharmacopoeia guidelines are adhered to. Pharmacopoeia are documents binding for a particular continent, e.g. American , Japanese, European, Russian pharmacopoeia, etc. American pharmacopoeia is the one of the greatest priority.
There are two chapters devoted to requirements concerning balances, and . The former one describes specification for repeatability and accuracy, the description is as follows:
Repeatability is satisfactory if two times the standard deviation of the weighed value, divided by the nominal value of the weight used, does not exceed 0.10%. If the standard deviation obtained is less than 0.41d , where d is the scale interval, replace this standard deviation with 0.41d
The accuracy of a balance is satisfactory if its weighing value, when tested with a suitable weight(s), is within 0.10% of the test weight value. A test weight is suitable if it has a mass between 5% and 100% of the balance's capacity
Chapter 1251 is not compulsory, it supplies the reader with explanation and definitions of terms that are pivotal when it comes to electronic weighing equipment:
sensitivity
accuracy
linearity
eccentricity
In order to comply to regulations of pharmacy industry it is necessary to meet chapter 41 requirements, especially those intended for repeatability of indications. As it is commonly know, it is repeatability that decides on measuring accuracy, i.e. balance reliability. For microbalances this parameter is used for MSW determination.