Interested to Buy Any Domain ? << Click Here >> for more details...
what do you mean by Q+5 in dissolution
- 1 Answers
- 25240 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 |
What is the process validation?
what is difference between in drug purity and drug potency
What is your work experience in pharmaceutical field?
hi i have done my b pharma and now i am working as a managing director in my own manufacturing unit is there any scope overthere 4 me
If you have given an unknown compound how you develope a hplc analysis method for anlysis?
4 Answers Aurobindo, Glenmark, Mylan, Torrent Pharma, Vivimed Labs,
difference b/w sonication and homozinization?
hai,i had completed my b.pharmacy.i want the coaching centres for drug inspector exam at hyderabad,pls help me nd wen wil b the DI exam conducted in 2012 mostly,pls also forward the model papers.. pls reply me at pravaliden@gmail.com
what do you mean by bracketing and matrixing in stability
basic of hplc,columns used
What do you mean by LOD and water content?
Whhat is the justification for stability study in api missed stations through deviations and statistical analysis is required.
What are the advantages and disadvantages of working for a small & big pharmaceutical company?
Pharmacy 
