Which is the best Institute for Clinical Research, Clinical Data Management and Pharmacovigilance in Hyderabad?
5 6981Job oriented Training in Oracle Clinical, CDM, Clinical Research and SAS with Clinical Trails
1 4528how to calculate potency of working standard by using mass balence method & this calculated potency is on as basis or on anhydrous/ dried basis
8220If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can u proceed calibration?
2953Post New Health Pharma AllOther Questions
What is the basic requirement for preparing drug master file , like EDMF , USDMF ?
What r the different sop in or plant
what is the leak test procedure of filled bottles (liquid)
Tell us about a time when you failed to meet a deadline. What were the repercussions?
why you are become a medical representative
why nitrogen charecter as a inert gas plz identified
what is the mechanism of action of local anaesthetics?
What is the role of buffers (ex: KH2PO4) in HPLC analysis,
How are you qualified for the position of Assistant Clinical Director?
How to perform forced degradation on tablet sample or suspensions?
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.
What is forced degradation study?
Tell us about a situation in which you took the extra step for a patient.
How to preform dissolution profiling
how many clauses are there in iso? give me the clauses details?
