what do you mean by Q+5 in dissolution
- 1 Answers
- 24380 Views
- I also Faced
- E-Mail Answers
Answer / suresh naidu
Q is the specification limit( the mean of individual tablets tested should be not less than Q) of the dissolution test.
Q+5 is the criteria for which the dissolution passing with 6 tablets at S-1 stage (optimum release).:
| Is This Answer Correct ? | 41 Yes | 4 No |
i am pursing b.pharmacy iam interested in applying for the post of drug inspector piz give me ideas how to pepare and if you have model papers plzzzzzzzzzzz do send me sir my email id is vishwanreddy_90@yahoo.com
how we can fix re-standardization due date in volumetric solution
what is the calculation for getting the tablet weight and the punch size, Eg..if there is a 8/32 punch then how to measure tablet weight????
What do you mean by Bracketing and Matrixing in stability?
what is purpose of slow,medium,fast sampling in process validation ?
what is difference between uv , pda & ri detector ?
Why 3X samples collected in process validation?
What is stationary phase?
how much the minimum recovery should be in swab sampling
why u have low score in toefl
what is capacity factor
in performing of disintigration test in wich condition we use the disc&in wich condition we nt use the disk clarify wit reasn?
Pharmacy 
