How To conduct Clinical Trials

Clinical trials or clinical research studies, to tests the potential treatments in human volunteers to see whether they should be approved for wider use in the population. In the examine a treatment could be a medicine, medical device, or biological or gene therapy. Potential treatments, however, must be studied in laboratory animals first to control potential toxicity before they can be tested on anyone or patients. Treatments having acceptable safety profiles most promises are then moved into clinical trials. Although the word new may imply betterment, it is not known whether the potential medical treatment offers to patients until clinical research on that treatment is complete. Clinical trials are an integral part of new product discovery and trials before a new product can be brought to the market. The organization is committed to protecting the participants of clinical trials, as well as providing reliable information to those interested in participating. Recently, unethical behavior on the part of some researchers has rolled the public trust and prompted the regulations and guidelines for clinical research and trials to protect participants from unreasonable risks. Although efforts are made to control risks to clinical trial participants, some risks may be unavoidable because of the uncertainty inherent in clinical research involving new medical products. It's important, therefore, that people make their decision to participate in a clinical trial only after they have a full understanding of the entire process and the risks that may be involved.

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