MBBS/MD/BDS/ BHMS Project – BioMed Informatics Hyderabad
Clinical Trials & Clinical Data Management - CDM Project Biomed Informatics Hyderabad
BioMed Informatics
Medwin Hospitals Academic Wing, Ist Floor,
Medwin Hospital, Nampally, Hyderabad – 500 001
Phone: 040-40209750/66821025
Project Title:
Clinical Trials & Clinical Data Management - CDM
Eligibility:
MBBS, MD,BDS, BHMS, BUMS, BAMS, BPT
M.Sc., (Microbiology/ Biochemistry/ Biotechnology/ Bioinformatics/ Chemistry/ Genetics/ Botany/ Zoology/ Life Sciences/ Nursing)
B.Pharmacy, M.Pharmacy, B.Sc., B.Tech.(Biotechnology)
Introduction to clinical Trials & Clinical Data Management
The study design that provides the most compelling evidence of a causal relationship between the treatment and the effect, is the randomized controlled trial. Studies in epidemiology such as the cohort study and the case-control study are clinical studies in that they involve human participants, but provide less compelling evidence than the randomized controlled trial. The major difference between clinical trials and epidemiological studies is that, in clinical trials, the investigators manipulate the administration of a new intervention and measure the effect of that manipulation, whereas epidemiological studies only observe associations (correlations) between the treatments experienced by participants and their health status or diseases.
Currently some Phase II and most Phase III drug trials are designed to be randomized, double-blind, and placebo-controlled.
This means that each study subject is randomly assigned to receive one of the treatments, which might be the placebo. Neither the subjects nor scientists involved in the study know which study treatment is being administered to any given subject; and, in particular, none of those involved in the study know which subjects are being administered a placebo. It has become a common practice to conduct “active comparator” trials (also known as “active control” trials) – in other words, when a treatment exists that is clearly better than doing nothing (i.e. the placebo) for the subject, the alternate treatment would be a standard-of-care therapy.
Pharmaceutical clinical trials are commonly classified into four phases, and the drug-development process will normally proceed through all four stages over many years. If the drug successfully passes through the first three phases, it will usually be successfully approved for use in the general population. Before pharmaceutical companies start clinical trials on drugs, extensive pre-clinical studies are conducted.
How To Apply:
To apply and for more details regarding project , candidates are kindly requested to register their names in the website
source:
www.biomedlifesciences.com
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