Answer / gokulcharan

Assay Means Quantitatively determination of the amount of
MAin component of a sample present in substance.

Answer / kanakadurga

how much amount of api[active pharmaceutical
ingradient]present in the given sample can be analysed
through assay.

Answer / subodh

Purity of labeled content amount

Answer / bhupalreddy

A quantitative or qualitative test of a substance
(especially an ore or a drug) to determine its components;

An analysis of the composition or strength of a
substance, esp. a determination of the amount of metal in
an ore, alloy, etc.

Answer / raja.s

Quantitative determination amount of main compound sample present on substances.

Answer / rajeev ranjan

Quantitative Determination of Purity of Sample.

In Stability testing if significant change occurs then what will be the action plan?

2 Answers   Cipla,

What is similarity factor and its use in api strength?

0 Answers  

What will be the effect on HPLC analysis result if three mobile phases given separately through three valves and same proportion mixed together and given by one valve?

1 Answers   LOIL,

Describe your experience with quality assurance and quality control analyses?

11 Answers   Aurobindo, Dr Reddys, MSC, Reddy Labs,

What is the defination of Bulk density?

4 Answers   Dr Reddys,

Why triethylamine and o-phosphoric acid used while setting pH of mobile phase during HPLC Analysis?

6 Answers   Hapten Healthcare, Pharmaceutical,

in each media we require to use SLS? how to proceed?

0 Answers  

differance between L1 and L7 columns

5 Answers   Everest,

How can we separate Urea & semicarbazide in single HPLC method ?

2 Answers  

What is (Q) point dissolution?

6 Answers   Cipla, Macleods,

If compound Pka is 5 then which buffer you will select ?

5 Answers   Avra, GVK,

in hplc calibration we are using 0.05% acetone why we are using that one and what happen when its conc increases or decreases

4 Answers   Aurobindo, Cadila, Martin,