What do you mean by CAPA?2 5808
In KF Standardization why we use Disodium Tartarate?1 4613
What is the difference between Deviation and Out of Specification?1447
What is the difference between mix-up and cross-contamination?1 4829
What is GMP, cGMP and GLP?1 10031
How polarimeter is calibrated?1 998
How melting point apparatus is calibrated?1 4681
What is the difference between uniformity of content and content uniformity as official test for all tablets?1241
What is limit of uniformity of content as per USP?3 3106
What do you mean by Q+5 in dissolution?
What should be the minimum limit of a working standard?
What is the difference between temporary change control and deviation?
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 firstname.lastname@example.org
principle of dissolution
What exepients are used in dry powder injections?
how quantitative stability studies are done?
why we use matrixing method in stability study and on what basis time points are selected?
How we fix the validity period of a volumetric solution and re-standardization due date?
When we change water of Hygrometer?
What should be Step wise the sterlization procedure for Dry Powder injection facility (from Starting)?
if one drug is acidic in nature and the other drug is basic in nature, e.g. desloratadine is soluble in acidic environment i.e 0.1N HCL whereas Montelukast Sodium is soluble in basic environment i.e. .2% SLS. How can we choose a common media for there Dissolution?
How to select HPLC column for a particular product?
what is difference between uniformity of content and content uniformity as official test for tablet
How can you fix the known and unknown impurity limit for any drug substance?