Clinical trial is conducted bring the new drug, treatment or the procedure to improve the human healthcare. As the outcome of the study is going to affect the health care of the mankind globally, it is never biased by the opinion of the individual, it always an outcome study by the group of experts for particular period of time. Concluding the clinical trial does not happen in a day or two, it demands certain period of time and also is an expensive affair. It is collaborative effort of medical knowledge and the finance. Whom does the medical trial include?
- Sponsor, the key person for initiating the process of the clinical trial, it is generally the manufacturer of the product. The product once manufactured in the organization is said to get the approval from the FDA, the reason why the clinical trial is conducted. Sponsors many include the pharmaceutical industries and the government agencies.
- Investigators, the experts responsible for conducting the clinical trial and documenting the outcomes of the study.
- Volunteers are the patients who actively take part in the clinical trial giving their consent.
- IRB is an independent committee of the doctors and analysts to ensure that the conducted medical trial meets the specified ethics and respects the rights of the participants.
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