In Stability testing if significant change occur then what is the action plan?4 16452
1.why did you choose this career 2.what is pharmacists ideal job1430
why you choose pharmacy as a career what is pharmacists ideal job what is your goal in ur profession and how you achieve it952
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 me816
Can any deviation be changed into the change control?1 3598
What is the difference between Humidity and Relative Humidity?2 5215
What do you mean by MKT (Mean Kinetic Temperature) in stability?1 4701
What are the stability zones and stability conditions?1 1834
i am preparing for Drug inspector exam.If u have previous questions please send me.
when will andhara pradesh government announces drug inspector posts and when will be the exam conducted? please inform me..
at what interval Ukrainian audit will come once you register your product??
what is difference between usfda and mhra guidline
if calibration of 12 bowl dissolution apparatus does not meet a single stage procedure how you can proceed calibration
How to select temperature of ODT in disintegration test
define the starting material?
What is pooled sample and why it is required in dissolution test?
when we calibrate uv for control of wavelength we scan for 200 to 800 nm but we get the result only for some specific wavelength how we confirm for all other wavelength?
What is column efficiency and performance ? And how can we know the column is better?
What is the Disintegration time for Hard gelatin Capsule in USP?
what is recovery factor
Hi, I am studying Bpharmacy final year. 1)I want to interview questions for facing basic interview.please help me to provide model papers for all pharma companies and give ur valuable suggestions also. 2)Send me important links for BPharmacy interviews. 3)How should i prepare for facing interview,please give me suggestion. My email id:firstname.lastname@example.org
If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can you precede calibration?
How can you fix the known and unknown impurity limit for any drug substance?