Interested to Buy Any Domain ? << Click Here >> for more details...
Why 3X samples collected in process validation?
- 3 Answers
- 13363 Views
- Cipla, I also Faced
- E-Mail Answers
Answer Posted / chaitanya patha
1 for QA , 2 for QC , 3 for Future reference in case of any
problem that may arise with the batch after its release into
market.
| Is This Answer Correct ? | 12 Yes | 15 No |
Post New Answer View All Answers
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 is pooled sample and why it is required in dissolution test?
hello,am milan mohite,i have completed B.PHARM,in 2008.and now do M.B.A from ignou,and D.P.P.M,from IPER{PUNE},please suggest me best coaching institute in pune for drug inspector,and send me model question paper for prepration of D.I. on my e.mail id - milan_mohite@yahoo.in Thanks.
Why we use 10 tablets for the analysis of cu test?
why we use matrixing method in stability study and on what basis time points are selected?
why we are using toluene in resolution in UV calibration
Delay in receiving offer letter? Dear All, Recently I clear all technical and HR round with one good MNC. I've submitted my scan document of qualification and work experience. Evenafter 2 weeks of sending documents, they didn't release the offer letter. Please suggest me effective email contents to deal them. Thank You
What is the difference between Analytical method validation and Analytical method transfer?
plzzz..send me the pevious papers of drug inspector for uppsc....i.l b highly oblige
Can you please mail me the latest syllabus of UTTAR PRADESH DRUG INSPECTOR entrance exam and UTTAR PRADESH FOOD INSPECTOR entrance exam with the eligibility criteria for Uttar Pradesh domicile candidates.
How we define validity of any Reagent , Indicator and Volumetric Solutions
What is difference between assay and content uniformity ?
What is column efficiency and performance ? And how can we know the column is better?
How can you fix the known and unknown impurity limit for any drug substance?
what is purpose of slow,medium,fast sampling in process validation ?
