Interested to Buy Any Domain ? << Click Here >> for more details...
Answer Posted / bvk
Out of specification
Deviation
| Is This Answer Correct ? | 0 Yes | 0 No |
Post New Answer View All Answers
calibrtion procedue of LC-MS
which batch require to use for analytical method validation?
WHAT IS THE PARAMETER FOR THE SELECTION OF MOBILE PHASE IN HPLC?
Which parameter require to do for analytical method equivalency?
give clarity of linearity and range in method validation
what is mean by nitrosamine impurities?
Which is the highly polar and highly non polar column in HPLC?
What are usp limits for theoritical plats,resoution,tailing factor,peak to valley ratio
why multimedia dissolution require to do?
If vendor having more imp than monograph then how to proceed? and how to set spec?
How you develop a method in HPLC?
about method developement in hplc
what is difference in ods I ods II is this is realy from sorbent / packing characteristics or from other means
before starting analytical method valodation what you checking? and how giving preference to start validation?
In BP2013, Loperamid HCl monograph. Assay by titration with 0.1N sodium hydroxide using hydrocloric acid 0.01N and reading the volume added between the 2 points of inflexion. I have a question that if the diluent solvent is ethanol is certainly consumed a amount of volume of titrant, so this volume must be eliminated on the result calculation or not apart from first point which is subtracted above.
