If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
311analytical method validation require to with respect to release specification or shelf life specification?
280in monograph 7 imp are there but in vendor showing 5 imp do not req to include 2 imp for that what will be justification?
265In which situation we require to prepare the standard solution from sample in Related substance method?
287Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
278
What is a synthesizer?
Explain what is a crest?
How can sedimentary processes concentrate and form resources? Give an example of a resource formed by a sedimentary process.
Define the phenomenon catenation. Which element has maximum catenation ability?
What are polyclonal antibodies?
What are isotypes?
Which is the biggest land animal?
How do you calculate tensile strength?
How are animals classified according to the germ layers present in their embryonic development?
can we re-freeze the 4% paraformaldehyde for longer storage?
Explain your experience with soil and water conservation practices and your role in preventing erosion and maintaining soil health.
Macrophages, which are present in the connective tissue, are called as.
what is the exact classification of pharmaceutical industry (area wise) as per cleaning limits(Class A.B.C.D)
How does the diffusion equation differ from the cable equation?
What is the most abundant form under which nitrogen is found in nature?