Questions
Clinical Trials volunteers provide a valuable service to the community to help researchers advance medical science and improve healthcare for future generations.
Why do we need Clinical Trials?
Without Clinical Trials, all the medicines and treatments we have today would not exist. To develop new treatments that are both safe and effective, tests must be performed.
The Food and Drug Administration (FDA) requires that all medical treatments or methods be vigorously tested to ensure that they are both effective and generally safe.
Clinical Trials volunteers provide a valuable service to the community to help researchers advance medical science and improve healthcare for future generations.
What is a Clinical Trial?
A Clinical Trial is a study designed to provide valuable data for a new or existing treatment or treatment method to determine if it is safe and effective for humans. To determine whether a treatment is both safe and effective, tests must be performed to provide statistical evidence. According to laws and regulations,
All clinical trials must be reviewed, approved and monitored by an Institutional Review Board (IRB) to ensure ethical treatment of participants and to ensure that all participants are fully informed about the study before agreeing to participate.
After you have been able to ask all your questions, the investigation procedure is clear to you and you have been able to think about it, you will be asked to sign an informed consent.
Who can participate in a clinical trial?
Each Clinical Trial has specific criteria regarding the type of participants required for the study. These criteria exist to ensure that good statistical data can be collected for the research.
You as a participant must therefore meet the inclusion criteria in order to participate in a project.
How does a clinical trial work?
The very first thing that happens when you choose to participate in a clinical trial is that you get a full explanation of the study, potential risks and benefits of the study are discussed with you. If you agree to participate in the study, you can always stop participating at any time.
The purpose of the study is to collect valuable data from you that directs the results of the study.
What questions do I have to ask before participating?
Volunteers are always fully aware of study requirements, required visits, tests, procedures, etc. In addition, volunteers are always informed of known or probable risks of a study or new risks discovered during the study.
You must ask all the questions you have before making the decision to participate in a study. Make sure that you know exactly what is required of you and that you are willing to perform the required tasks in the investigation.
Also make sure that you understand the benefits and risks of the study and that you can accept the risks of participating.
One of the most important things to remember is that participation in a clinical trial is always on a voluntary basis that you can terminate your participation at any time.
Are there any costs associated with the research for me?
No, a clinical trial is sponsored by the pharmaceutical industry or the government
Are you interested in participating in an ongoing investigation or do you want to register in our patient database without obligation? Then we look forward to your commitment!
If you are interested in participating in clinical trials or if you want more detailed information, you can register with us.
We hope that we can find a suitable study for you now or in the future.