Interested to Buy Any Domain ? << Click Here >> for more details...
Answer Posted / ashok linge
Impurities are substances inside a confined amount of liquid, gas, or solid, which differ from the chemical composition of the material or compound.
| Is This Answer Correct ? | 2 Yes | 0 No |
Post New Answer View All Answers
What is the difference between spectro meter and spectro photo meter?
Why dissolution test is not performed in all of the products
WHY given much noise PDA dector then VWD Dector
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
Why do we use KMnO4 in the test of control of obsorbance ? and why do we take specific quantity i.e 57-63mg?
WHAT IS THE CRITERIA FOR SELECTION OF TIME OF DISSOLUTION AND THE MEDIUM OF DISSOLUTION?
what is mean by extactable and leachable study?
in sampling of raw material which side is pasted sampled labels
how to get accurate result for Residue on evaporation in purified water
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.?
Why use only methanol,used determinationof moisture content not use other solvents
what is biorelivent dissolution media?
how to decide for one product require water content or LOD?
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 which situation we require to analytical method validation of excipient?
