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Chemistry AllOther (190) If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
824analytical method validation require to with respect to release specification or shelf life specification?
853in monograph 7 imp are there but in vendor showing 5 imp do not req to include 2 imp for that what will be justification?
786In which situation we require to prepare the standard solution from sample in Related substance method?
827Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
759
acceptance criteria for lod & loq by standard deviation of response and slope??
What makes a molecule into organic molecule?
What is the application of hardness date in environmental engineering practice?
in which situation require to use paddle and basket?
Why ammonia is used as buffer solution in estimation of copper by EDTA method
inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?
How can we confirm the HPLC column is end-capped or not? Is it possible to identify by physical appearance?
if your product is soluble in 0.1n hcl and water then which you choose as media from these 2 media?
What is stray light in uv what are units for stray light
What are hard waters?
what are UV rays absorbs slightly?
What is colorimetry?
Acid value definition is number milligrams of koh required to nuetralise the acid present in one gram oil & fats but why not use naoh for nuetralisation?
how you start RS method development when for new product?
Why is the color of the indicator drop remains the same at the end point?