how to start the method development of Dissolution and related
substances.
Answer / satheesh kumar
Dissolution-Amount of drug release in solid dosage form in
different media.
In dissolution run time should be less,time points are more
(5min,10min,15min,25min,30min and so on)for a single
batch.Primarily check the available impurities not co-elute
with our drug product.
In related substances we are considering about known and
unknown impurities.
| Is This Answer Correct ? | 4 Yes | 6 No |
what is the criteria for choosing capillary column in GC??is it dependent on sample load?
what is the identification test of volatile substance? what is volatile compound?
what is least count of a balance? How we find out this? Any formula for least count of Analytical balance?
13 Answers Acme Formulation, Analytical Solutions, Dr Reddys, Reddy Labs,
What is the diffrence in japan mkt requirement in analytical method validation over US?
we are performed SOR for a particular product the limit is -6 to -10.We face particular bathes it is not meeting the specification.we performed diffrent instrument diffrent analyst we are getting diffrent diffrent results.solvent is dimethyl sulfoxide what could be the reasion
why 1.2%kcl solution is using in limit os straylight?and why this test used for uv calibration?
1 Answers Graviti Pharmaceuticals, Reddy Labs, Vimta Labs,
Why we compare unequal concentrated solutions in heavy metals test. For example comparing the test solution with 1 ppm lead standard and telling it's less than 20ppm?
1 Answers Micro Labs, Mistair,
a bottle of concerntrated HCL (36.5) was labelled as 37% (w/w) and density 1.19m/l.What is hcl molarity?
What is FFA, PV, and PAV value in oil.
what is mean by extactable and leachable study?
What are the class-1 residual solvents listed in ICH guidelines?
mahagenco syllabus for the post of chemist
0 Answers MahaGenco, Unimarck Pharma,