Why dissolution apparatus having 8 jars ?
- 5 Answers
- 14793 Views
- I also Faced
- E-Mail Answers
Answers were Sorted based on User's Feedback
Answer / sourabh pandit
6 for tablets sample
1 for placebo
1 for media replacement
| Is This Answer Correct ? | 19 Yes | 1 No |
Answer / txuan
6 for testing tablet sample
1 for reference sample
1 for placebo sample
| Is This Answer Correct ? | 5 Yes | 4 No |
Answer / arvind kumar singh acme formul
6 tablets or capsules
1 copnset
2 placebo
| Is This Answer Correct ? | 1 Yes | 1 No |
Answer / rakesh vishwakarma
6 for testing tablet sample.
1 for blank
1 for placebo.
| Is This Answer Correct ? | 0 Yes | 2 No |
Why KBr is used in FTIR ?
how a particular wavelength can be different for a particular compund while analysing by uv and by HPLC.
How to set analyticl specification for combination products?
Difference between related substances & impurities
why don't we call POH meter? As we all as PH meter
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 we are using 6 dosage units in dissolution, and why we are using 6 tablets in disintegation test.is there any scientific reason beyond 6?
1.What is the difference between method validation and method verification 2.Which guidelines proposed to method transfer
If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
IF THE COMPOUND PKA IS 5.3 WHY WE ARE ADJUSTING PH+/-2 OF THE COMPOUNDS PKA. WHAT IS THE CONDITION
2 Answers Dr Reddys, Reddy Labs,
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
what is difference between assay&purity&potency?
Organic Chemistry 
