whem will be the exam or interview for the post of Drug inspector is conducted in jammu and kashmir??? the form was filled on starting of 2013.
1964while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that
2071why assay test and loss on drying test should be performed on same day during raw material analysis??
1 4052Can 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.
1966Anyone have any idea when to conduct Uniformity of Weight (UOW) and when need to conduct Uniformity of Dosage Units (UOD) or when need both? I read BP it only said if average weight < or = 0.04g then just conduct UOD, no need UOW. Under UOD section, it doesnt say when need to conduct UOD but just said UOD got two type, one is Mass Variation (MV), another is Content Uniformity (CU) and under what conditions to conduct them. For USP, no UOW section, only got UOD section.
2233using of chemical standards in HPLC he customer gave 100.2% what potency i will use this potency in hplc?
1 2793
How should the Medical Librarian interact with training staff?
plz send me previous model question paper for moh to my mail plz it's urgent my mail id is zeeta_lobo@yahoo.com
What are the different techniques for placing samples in micro-scope?
What is the difference between Analytical method validation and Analytical method transfer?
why we have to use particular buffer only for dissolution.
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 some samples are taking 500mg for water content and some samples are taken 2g for water content?
how many clauses are there in iso? give me the clauses details?
If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can you precede calibration?
what is the range of ftir as per usfda?
IN OOS SAMPLING ERROR HOW CAN WE ADDRESS , OR HOW CAN WE EXPLAIN AUDITOR ABOUT SAMPLING ERROR
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
Which disease occurs due to the deficiency of vitamin "d"? What are its symptoms?
what is the difference of vaccum pressure and vapour pressure ?