Clinical research is a type of study of clinical or biomedical questions through the use of human subjects. Clinical research studies do not necessarily all involve medical treatments or experimental therapies. Clinical research can include observational studies, in which people are followed over a period of time to determine health outcomes. Clinical research may also be used to determine the usefulness or safety of a new diagnostic procedure or drug treatment.
What happens to drugs that don't make it out of clinical trials?
Most drugs that undergo preclinical (animal) research never even make it to human testing and review by the FDA. The drug developers go back to begin the development process using what they learned during with their preclinical research. Learn more about Clinical Research Courses.
Phases of a Clinical Trial
There are several stages, or “phases,” of a clinical trial. Each new phase builds on information from previous stages.You might qualify for a certain phase of a trial because of the state of your health or the seriousness of your particular illness. People who take part usually do it in phase III or IV of the trial.Talk to the clinical trial coordinator to find out which phase the clinical trial is in. Learn more about the different clinical trial phases and whether they are right for you.
The most commonly asked question by the volunteers of any clinical trial recruitment process is the protection given to them. There are a number of measures that are taken to ensure that the participants of the trial are well protected and safe during the trial. The concerned authorities constantly review the protocols of every trial to ensure that it is done ethically and the patients' rights are protected. Apart from this, the FDA provides oversight for clinical trial testing of medical devices or drugs. Prior to human clinical trials, the FDA reviews the applications for the new treatments and medications to ensure that the studies and researches have protections in place for the volunteers. The completely informed consent forms of the patients are one of the most important pieces of the puzzle of any clinical trial that protects the volunteers. Any changes in the mind of the volunteers enable them to withdraw from the trail immediately, ensuring their complete safety.
Conclusion
Clinical research trainings are given to every professional involved in the trial. Clinical research courses are continuously updated based on the disease and development of technology to ensure the complete safety of the participants of the trial.
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