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Answer Posted / yogi
no functional grops in kbr
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How can I develope method of dissolution by HPLC OR UV
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.?
What is the purpose of octyl silane columns?
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?
what is the purge flow & how to calculate
While performing TOC sst analysis Zero shift disabled & sample analysis zero shift enabled why?
WHAT IS THE USE OF STARTER ?????????
which are the diffrent batches in the pharmaceuticals?
for inorganic molecules require to do RS, Assay and disso?
what is turbidimetric titration?Give 2 examples.
How can the GC or HPLC method is selected to determine the impurity profile in drug product?
Which parameter require to do for analytical method equivalency?
How to set analyticl specification for combination products?
Why we select scan range from higer wavelength to lower wavelength in uv visible spectroscopy and ftir spectroscopy ? .
why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?
