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No, the investigator should not give a copy of the Investigator's Brochure (formerly known as the Investigator's Clinical Dossier) to trial participants. The Investigator's Brochure is intended for the investigator's reference to ensure they have a comprehensive understanding of the investigational product being studied. Providing this document to participants could pose potential risks such as confusing or misleading information. Participants should instead be provided with an informed consent form that includes relevant details about the trial.
Clinical Trial Data Services (CTDS) are an organization that focus on clinical research. The organization also provide understanding about clinical trial processes, for example.
What should be included in a clinical trial
Clinical Trial Service Unit was created in 1975.
The clinical trial management system is used in biochemical, pharmecutical industries and clinical research institutions. The system itself is used to correlate large amounts of data concerning the clinical trial.
If this pertaining to a clinical trial that you're participating, then I suggested that you contact the study investigator. The investigator contact information is usually written in the consent form that you signed in the beginning of the study.
You would register for clinical trial patient treatment by contacting a company that specializes in the recruitment of people for clinical trials. One such company is called Clinical Connection.
What are the pros and cons of independent members in clinical trial committees having volunteers in these positions
Clinical trial management software helps in the process of recording various medical results obtained during the clinical trial phase of medical testing.
An actual patient
Hospital costs
There is very little cannibalism in clinical trials