Weight balance variation limit during analysis
- 7 Answers
- 8259 Views
- Amneal Pharmaceuticals, I also Faced
- E-Mail Answers
Answers were Sorted based on User's Feedback
Answer / srinivas
Balance variation for analysis 10% for both solids and liquids according pharmacopoeia
| Is This Answer Correct ? | 21 Yes | 0 No |
Answer / neeraj
Balance variation limit is 10% for solid as well as liquid
| Is This Answer Correct ? | 3 Yes | 0 No |
Answer / penchal reddy
As per USP Below 100 mg weighed 10%
Liquids 10%
| Is This Answer Correct ? | 0 Yes | 0 No |
Answer / kambam raveendra reddy
for solids 5% and for liquids 10%
| Is This Answer Correct ? | 1 Yes | 9 No |
How precise should be the linearity in HPLC method validation?
What are usp limits for total impurities,unknown impurity
Why we are using K2Cr2O7 for control of absorbance in UV?
Whya the need of Specificity to do in Analytical Method Validation ?
IN DISSOLUTION WE ARE USING A LETTER 'Q' WHAT IS MENT BY Q
5 Answers Reddy Labs, Torrent Pharma,
What is polymorphism?which type of compounds exhibits polymorphism?
perchloric acid&glacal acetic acid both are acids but reaction is complete in volumetric titrations.how?
What is discriminating media? How can u justify/select that which media (pH etc...)is suitable for your dissolution study of your compound?
what is specificity?
4 Answers Amneal Pharmaceuticals, Aurobindo,
why salicylic acid not use for dissolution.
2 Answers Cipla, Indo Baijin Chemicals,
what is optical active and non active give examples?
What is cleaning validation of rinse and swabe and its limit with caculation formula.
Organic Chemistry 
