Answer Posted / chaitanya
It was performed in order to ensure that any degradants generated during storage and shipment will not influence the assay of the method or the peak of interest. This is the reason why we are to acquire 10 to 30% degradation and peak purity should be passed
| Is This Answer Correct ? | 2 Yes | 0 No |
Post New Answer View All Answers
4. Describe the operation of the Craig apparatus. Chapter.3 Equilibrium Processes in Separations
What if impurity area in control sample coming more as compared to LOQ level of impurity ?
What is delay volume?
pharma industries oriented
AT WHAT CONDITIONS WILL YOU ANALYSE A SAMPLE,WHICH ARE PRESERVED AT OTHER THAN THE AMBIENT CONDITIONS?(ie COLD STORAGE SAMPLES BELOW 20* CENTIGRADE?
What is intact assay method development.....?
What is dose dumping? why require to do?
WHAT IS THE PARAMETER FOR THE SELECTION OF MOBILE PHASE IN HPLC?
how can give the expiry period and restadardisation of volumetric solution
How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?
Describe your field experience sample type collected,sample techniques,field measurements taken and equipment used?
How to fix the sample conc. in Related substances test by HPLC?
How to set analyticl specification for combination products?
Identify problem faced when mass spectroscopy is used with HPLC system ?
What is the main difference between ODS1 and ODS2 Hplc column.
