From where require to take the RLD sample?
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In pharmaceuticals formulation OOS applicable in Raw Material(which is not manufacturing in the company. and purchase by approved vendor)).Why?
what is the moisture content of Disodium hydrogen tartrate. how it can be calculted. as 16.5%
[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?
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?
In case of dissolution test, if there is variation within 6 individual units however the batch is complying as per S1 criteria, is it necessary to do investigation for the same? What should be the criteria for such variation?
how peak can be sharp in hplc when it is come flat
6 Answers Graviti Pharmaceuticals,
In Stability testing if significant change occurs then what will be the action plan?
What r the limitatoins of uv visible spectroscopy ? Why Water use in blank standard for uv visible spectroscopy ?
why using the ph 4,7,9.2?
From where 16 or 5.545 is derived in theoretical plates calculation formula by USP or JP/BP/DAB and what is meaning of this coefficient and impact in calculation ?
2 Answers Nectar Lifesciences,
What is difference b/w IR&NIR
how you establish the LOQ?