[3/28, 20:52] Manoj P Venkatpurwar: how many impurities require to inject in assay specificity that how we can find out? and in Rs also how?
how can give the expiry period and restadardisation of volumetric solution
How to set analyticl specification for combination products?
How do we get end points and how many end points are possible for citric acid and di-acid not theorotically answer should be given practically.
As per ICH related substances stability trend limit from initial to shelf life
How to decide assay range for non pharmacopeial API analysis by HPLC? Could you give me any reference for same e.g Guidelines or Paper publications?
How to choose the which salt is suitable for mobilephase
Please give idea about method development for cleaning method and how maco level establish
is it necessary to do HPLC calibration at wavelength 315nm if we are doing analysis at this wavelangth
For limit test of heavy metals in BP, Method C require that the substance is ignited at a temperature not exceeding 800 °C. Why confines such the temperature?
4. Describe the operation of the Craig apparatus. Chapter.3 Equilibrium Processes in Separations
What are usp limits for theoritical plats,resoution,tailing factor,peak to valley ratio
what is mean by peak intigrity?
what is mean by dissolution biowaiver study?
What is mean by PDR?