Interested to Buy Any Domain ? << Click Here >> for more details...
Answer Posted / priyanka
8 carbon
| Is This Answer Correct ? | 0 Yes | 3 No |
Post New Answer View All Answers
While performing TOC sst analysis Zero shift disabled & sample analysis zero shift enabled why?
Qc interview questions
Why use only methanol,used determinationof moisture content not use other solvents
As per ICH related substances stability trend limit from initial to shelf life
In Dissolution Test why limit is define Q+5% what is the role of +5%.
how to selecet an exact coloumn for an new molecule development by hplc how to select exact salt as buffer for new molecule development by hplc what is the the process to select the mode of saparation of compoundes by hplc what is the use of ph of buffer what is use of buffer,ph,organic phase,ans methods how the molecules get saparated in coloumn,
Which parameter require to do for analytical method equivalency?
Please give idea about method development for cleaning method and how maco level establish
How will u perform degradation study in detectors other thann PDA in HPLC Methodology
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 WE USE HCL, CHOPPER, BURNER, MONOCHROMATOR in AAS? PLEASE EXPLAIN BRIEFLY
cefoperozone and sulbactam inj. hplc test method
Why dissolution test is not performed in all of the products
for which product require to do content uniformity? what is limit of cu?
Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
