Un-Answered Questions { Health Pharma }

HOW TO PERFORM SATURATION SOLUBILITY IN DISSOLUTION METHOD DEVELOPMENT?

3262


IN OOS SAMPLING ERROR HOW CAN WE ADDRESS , OR HOW CAN WE EXPLAIN AUDITOR ABOUT SAMPLING ERROR

2091


why we have to use particular buffer only for dissolution instead of using cheap buffer.

2329


why we have to use particular buffer only for dissolution.

2483


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.

1964


while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that

2072


Can 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.

1966


please explain the job responsibilities of quality assurance..

1858


Anyone 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.

2233


Why mineral oil or light liquid paraffin is used for ir analysis

3465


what are the GLP activities to be followed for Oncology products

2323


When we change water of Hygrometer?

8106


from hplc chromatogram how can we say that calibration is needed now?

2095


Whhat is the justification for stability study in api missed stations through deviations and statistical analysis is required.

3134


what is the calculation for getting the tablet weight and the punch size, Eg..if there is a 8/32 punch then how to measure tablet weight????

5268