if calibration of 12 bowl of dissolution apparatus does not
meet a single stage how you can proceed calibration
Answer Posted / rambabu vattikuti
12 bowl of dissolution apparatus does not
meet a single stage go to out of calibration and investigate same 1) if any abnormal observed in instrument previously perform product analysis shall be perform calibrated dissolution apparatus and results compare previously report results .
2)if any abnormal observed in during analysis like time,filter the solution, volume, tablets problem reanalysis shall be performed without discrepancy.
after re analysis not met acceptance criteria immediately inform service engineer if identify the instrument problem point 1 follow
| Is This Answer Correct ? | 2 Yes | 0 No |
Post New Answer View All Answers
when will andhara pradesh government announces drug inspector posts and when will be the exam conducted? please inform me..
WHEN WILL GUJRAT GOVERNMENT ANNOUNCES DRUG INSPECTOR POSTS AND WHEN WILL BE THE EXAM CONDUCTED? INFORM ME AND ALSO EAMINATION DATE
what is difference between uniformity of content and content uniformity as official test for tablet
plzzz mail me question papers and syllabus of mpsc's and upsc's drug inspector's exam.and details whn da exm is going to be.. my e-mail id is shubhg_2007@yahoo.com.thanx..
what are all the parameters to be considered while applying bracketing and matrixing?where and all it is applicable?
How to select temperature of ODT in disintegration test
What should be the minimum limit of a working standard?
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 jyothipasam@gmail.com
How many types of impurites in Related compound test?
pharmacovigilance opportunities in Hyderabad
How to check the integrity of Sieve, Screen, FBD Bag?
How we define validity of any Reagent , Indicator and Volumetric Solutions
Why we are using propyl parabben in methanol in calibration of hplc for GPV test??
what is the exact classification of pharmaceutical industry (area wise) as per cleaning limits(Class A.B.C.D)
What do you mean by Q+5 in dissolution?