Interested to Buy Any Domain ? << Click Here >> for more details...
Which is the best Institute for Clinical Research, Clinical Data Management and Pharmacovigilance in Hyderabad?
5 9116Job oriented Training in Oracle Clinical, CDM, Clinical Research and SAS with Clinical Trails
1 5184how to calculate potency of working standard by using mass balence method & this calculated potency is on as basis or on anhydrous/ dried basis
9020If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can u proceed calibration?
3398Post New Health Pharma AllOther Questions
You will be required to interact with patients. Tell us about your previous experience with patients and how did you deal with the experience.
how many clauses are there in iso? give me the clauses details?
What r the different sop in or plant
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.
Do you think it is possible to rehabilitate?
what is your experience in medical continuing education.
Explain difference between sonication and homozinization?
What is the basic requirement for preparing drug master file , like EDMF , USDMF ?
what is meant by artwork review and handling procedure with an example?
please e-mail me the model of Tamil Nadu drug inspector question papers
How can I assign a retest date for solvents e.g. toluene, methanol, etc?
What is forced degradation study?
difference between RF and correction factor?
How to preform dissolution profiling
What do you mean by GTT? What are the effect of GTT on film coating.
