In any clinical research, a sample of blood or tissue will be taken from the specimen and then will be processed as a genetic analysis study. The involvement of the subject will be only to produce the sample, where the sample is the essential link among the subject, his/her medical records and the obtained medical report. The report is generated after performing sufficient genetic analysis on his/her sample.
The sample will be secured and not disclosed to anyone else, apart from the subject and his/her close relative (that too if the patient insists), the researcher, who has done the genetic analysis and sponsors for the research. All medical samples will be stowed, cooled, archived and sent to researchers. The privacy of the patient is maintained and is given utmost priority. Other procedurals, such as access to the sample, discovery of the gene, drug development and registration of the product are strictly kept secluded only for the concerned personnel. Therefore, there is a strict vigilance on the passing of information in this perspective.
The clinical samples collected are stored for specific processes and trials. The results obtained by these trials are then shared with the government authorities, who will give away orders to develop new and better medications.

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