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AMRITA AKHOURI

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RECENT POSTS: 

Phase 0 Trial





Reliability





Adaptive Dose-finding Design





Adaptive Seamless Design





Sample Size Re-estimation (SSR) Design





Group Sequential Design





Adaptive Trial Design





Bioequivalence Studies





Assessment of Bioavailability





Absolute Bioavailability Vs. Relative Bioavailability





Bioavailability





Biologics/ Biological products





Sample Size





Thalidomide Disaster (1962)





Sampling Process





Elixir Sulfanilamide Disaster (1937)





Difference between Case control study and Retrospective cohort study





Cross-sectional study Vs. Longitudinal study (research)





Longitudinal Research





Non-Probability Sampling Technique





Probability Sampling Technique





Sampling







Blogs on Pharmacovigilance, Clinical Trials, Drug Safety and similar subjects

Phase 0 Trial

Drug takes years to be available in the market for general use. It is an
expensive, time consuming and full of uncertainty process. It...

Reliability

Reliability is the degree of consistency between two measures of the same thing.
It checks if the same score is obtained or not when...

Adaptive Dose-finding Design

In a traditional design, all the key parameters are pre-specified and they will
be constant throughout the trial. This may lead to a...

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