Interested to Buy Any Domain ? << Click Here >> for more details...
why should we not dispatch the reprocess material to
export
- 1 Answers
- 9219 Views
- Ranbaxy, I also Faced
- E-Mail Answers
Answer / mahesh shinde
Because there may be chances out of specification of product
like increase in impurity than its limit.
| Is This Answer Correct ? | 6 Yes | 2 No |
If we get 100% assay of an Initial sample ,and the stability studies of the same sample got 90% dissolution result, and when the same stability sample was analyzed for RS studies no impurities was found . Where the 10% Active substance were gone during dissolution analysis.Please help me in getting the conclusion.
How to select HPLC column for particular product.
what are the limit of LOD and LOQ
Why we said Glacial Acetic Acid to Acetic Acid m
What is your work experience in pharmaceutical field?
Why we use pyrene in HPLC calibration ( UV-vis/PDA)
2 Answers Lupin, MSN, MSN Pharma,
How Many Tablet Should be taken for Measure Wt. gain before and after coating?
6 Answers Ambee Pharmaceuticals,
i like to know when is drug inspector exam 2009.and plz send me da question paper, interviev questions,and other details on my mail.id. shubhg2009@gmail.com. plz
i have completed my B pharmacy i am trying to attempt group exam i have no idea of which group to select,where to take coaching any body can help me pls
1 Answers Cipla, Ranbaxy, RC Reddy,
What is the difference between Analytical method validation and Analytical method transfer?
Describe how you would educate a patient about the proper use of Alprazolam, including dosing instructions, potential side effects, and the importance of follow-up appointments.
what should be minimum limit of working standard
Pharmacy 
