Answer Posted / manish
: An impurity that theoretically can arise during manufacture or storage. It may or may not actually appear in the new drug substance. Qualification: The process of acquiring and evaluating data that establishes the biological.
| Is This Answer Correct ? | 0 Yes | 0 No |
Post New Answer View All Answers
what is the relation between Total organic carbon and Chemical Oxygen demand?
Which wavelengths are visible to human eye?
4.0 liters of oxygen are mixed with 8.0 liters of nitrogen. Identify the solute and solvent in this mixture:
Why are the titration involving edta carried out slowly towards the end point?
Why is the color of the indicator drop remains the same at the end point?
Explain substituted hydrocarbon?
Why is starch indicator added towards the end point?
Why we use potassium dichromate in control of absorbance in uv region and copper sulphate in control of absorbance in visible region?
Define what is avogadro’s law?
How is the accuracy of the method determined?
How is librated iodine estimated?
Explain the structure of a dna molecule?
Mention a few advantages of photoelectric colorimetric determination.
How is temporary hardness be removed?
What is meant by ph of a solution?