The duty of the clinical supervisor is to ensure that the researcher and the applicant complete their respective duties when conducting clinical trials, that is, to regularly visit, supervise and manage the experimental bases before, during and after the trials.

Clinical inspector is a person with relevant knowledge appointed by and responsible for the sponsor, whose task is to monitor and report the progress of the trial and verify the data. They can usually be employed by nurses, pharmacists, doctors or professionals who have graduated from related disciplines.

Clinical supervisors of clinical trials are usually appointed by the sponsors and accepted by researchers. Clinical inspectors should not only have a certain medical background.

Participated in relevant knowledge training (drug research and development, clinical trials, GCP, sop, etc.). ), and have the scientific and clinical knowledge needed to correctly monitor the test. He should also be familiar with the test plan, test process and other related contents to ensure the correct supervision and guidance of the test process.

Extended data:

The whole clinical trial is divided into three stages: trial preparation, trial implementation and trial completion, and each stage has its own different work contents and procedures. After receiving the approval of clinical trial, the applicant can formulate the trial plan and SOP, and at the same time start to screen the trial base and select researchers.

Then, the applicant can independently or jointly draft the detailed rules of the experimental scheme, CRF, ICF, etc. , and discuss and determine the above rules at the subsequent researcher meeting, and then apply to the ethics Committee for ethical approval. After all the drugs and documents are ready, clinical trials can begin.