If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can you precede calibration?
How do you balance the benefits and risks of Alprazolam treatment when considering its prescription for an elderly patient with multiple comorbidities?
What is difference between assay and content uniformity ?
what we do when calibration of any instrument is fail ?
What is validation, validation protocol and validation master plan?
define the starting material?
what is meant by artwork review and handling procedure with an example?
Why 6 tablets are used in dissolution and DT test ?Is there any specific reason behind it ?
What is the principal of particle size analyzer?brief explain instrumentation?
if one drug is acidic in nature and the other drug is basic in nature, e.g. desloratadine is soluble in acidic environment i.e 0.1N HCL whereas Montelukast Sodium is soluble in basic environment i.e. .2% SLS. How can we choose a common media for there Dissolution?
Why GLP is followed in the lab?
what are all the needs or pre-requisites to perform project on bracketing and matrixing of stability products?
How to measure each & every tablets hardness in compaction force control system of compression machine?
What is difference between Warm and Lukewarm Water as per pharmacopia.
what is difference between uniformity of content and content uniformity as official test for tablet