If we have 5 strength which is not dose proportinate and excipients also diffrent in each strength then how we can proceed for Force degradation? and excipient are same but not dose propotinate the how FD?
800If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?
986how decide the clining method and cleaning method validation require for this perticular products?
755Post New Analytical Chemistry Questions
1)What's the meaning of Absorption,give a example. 2)What's the meaning of Adsorption,give a example. 2)what is the difference between Absorption and Adsorption.
in which situation require to take incident in validation?
if your product is soluble in 0.1n hcl and water then which you choose as media from these 2 media?
Ph meter can show more than 14 ph reading? Why ph range in between 1 to 14 only?
how to select short coloum and long coloumn for new molecule
How to start the dissolution development for unknown tab?
if tech transfer fails whay require to do?
If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?
Explain the relations between number of carbon atoms in alkanes and retention time ?
what is classification of elemental impurities? what is risk assement in elemental impurities?
i want model written test paper for the post of analyst in IOCL(indian oil corporation ltd) any one pls help me
How much is the standard area for glc analysis
what is difference between UV - VISIBLE MODEL NO like 1600,1601,1700 etc ? plz explain me
analytical method validation require to with respect to release specification or shelf life specification?
What is the difference between Discriminating media and DPDM(Dissolution Profile with Different Media)