Add to ORKGValidation of UV-spectrometry assay method for dissolution profile test for levofloxacine tablets was carried out. The evaluated validation characteristics were: specificity, linearity, accuracy, precision, and analytical range. It was shown than main validation characteristics meet the Russian State Pharmacopoeia XIII requirements
<p>Under conditions of the pharmaceutical industry intensive development and variety of oral drugs, ...
Three simple spectrophotometric and atomic absorption spectrometric methods are developed and valida...
The aim of this study was to develop and validate a simple, sensitive, precise and cost-effective on...
Validation of UV-spectrometry assay method for dissolution profile test for levofloxacine tablets wa...
The method was validated by ultraviolet spectrophotometry for the determination of levofloxacin 500...
The objective of this research was to develop and validate an alternative analytical method for quan...
In Mexico, Metformin (MTF) is an oral hypoglycemic drug that is part of the group of biguanides used...
A new method for determination of moxifloxacin in human plasma using HPLC with UV-detection is descr...
New, simple and cost effective UV-spectrophotometric method was developed for the estimation of orbi...
Introduction. The strategy of quality control of drugs provides for compliance with the requirements...
AbstractA rapid, specific and economic UV spectrophotometric method has been developed using a solve...
Abstract: A new simple, rapid and reliable UV Spectrophotometry method was developed and validated f...
A simple, fast and economic reversed phase high performance liquid chromatographic (HPLC) method has...
Introduction. The strategy of quality control of drugs provides for compliance with the requirements...
A simple, selective and precise dissolution method was developed and validated for the Mycophenolate...
<p>Under conditions of the pharmaceutical industry intensive development and variety of oral drugs, ...
Three simple spectrophotometric and atomic absorption spectrometric methods are developed and valida...
The aim of this study was to develop and validate a simple, sensitive, precise and cost-effective on...
Validation of UV-spectrometry assay method for dissolution profile test for levofloxacine tablets wa...
The method was validated by ultraviolet spectrophotometry for the determination of levofloxacin 500...
The objective of this research was to develop and validate an alternative analytical method for quan...
In Mexico, Metformin (MTF) is an oral hypoglycemic drug that is part of the group of biguanides used...
A new method for determination of moxifloxacin in human plasma using HPLC with UV-detection is descr...
New, simple and cost effective UV-spectrophotometric method was developed for the estimation of orbi...
Introduction. The strategy of quality control of drugs provides for compliance with the requirements...
AbstractA rapid, specific and economic UV spectrophotometric method has been developed using a solve...
Abstract: A new simple, rapid and reliable UV Spectrophotometry method was developed and validated f...
A simple, fast and economic reversed phase high performance liquid chromatographic (HPLC) method has...
Introduction. The strategy of quality control of drugs provides for compliance with the requirements...
A simple, selective and precise dissolution method was developed and validated for the Mycophenolate...
<p>Under conditions of the pharmaceutical industry intensive development and variety of oral drugs, ...
Three simple spectrophotometric and atomic absorption spectrometric methods are developed and valida...
The aim of this study was to develop and validate a simple, sensitive, precise and cost-effective on...