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 2401could u send me the model papers available for drug inspector exam.
Orchid, APPSC, MPSC, Drugs Inspector, PSC, KPSC Karnataka Public Service Corporation, MAH, Ranbaxy,
80 42585i am a final year student pursuing B PHARMACY. i want to be a drug inspector. so plz tell how can i step forward toward this. plz tell me what should i do
3 3745i completed b.pharmacy now iam preparing for drug inspector post so iwant a model question paper for that if it is there plz send me to my mail id
4 5393
In dissolution test why sample is withdrawn from top of the paddle and not less than 1 cm away from wall?
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?
If granules are over lubricated what defect arises in tablet compression how we solve this problem.
If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can you precede calibration?
Why should we not dispatch the reprocess material to export?
can anyone help me by sending me model papers regarding drug inspector exam entrance model papers if yes plz send me to my email if yes sravani_262000yahoo.com, sravs.potti@gmail.com
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
What is the relative response factor in related substances?
please tell me croscarmellose sodium usp Water-soluble substances calculation and give me exmpl
How can you fix the known and unknown impurity limit for any drug substance?
why dissolution multimedia profile of drug is important. what are the specifications for tablets ,capsules,powders etc
What do you mean by Q+5 in dissolution?
how quantitative stability studies are done?
How we fix the validity period of a volumetric solution and re-standardization due date?
What should be Step wise the sterlization procedure for Dry Powder injection facility (from Starting)?
