Clinical trial process is conducted to give the new treatment or the drug or the medical device to the open world. How would this typical medical process run, the question wondering in the brains of the outside world.
The participant will be asked to sign the informed consent by understanding the content of the informed consent. Any clarifications regarding that will be provided by the medical trial co-coordinator or the medical expert. Once the informed consent is signed, the volunteer participant would undergo the medical screening to make sure that he/she fits in the credentials of the clinical trial. If the patient passes the medical tests she/he will be given the medicine and will be asked to reach the location for the next scheduled treatment. The information regarding whether the participant is undergoing a placebo treatment will not be disclosed to the patient. In the clinical trials the patient can enjoy the facility of quitting the medical trial process at any point of time.
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