Frequently Asked Questions:
1. What are the steps required to qualify and enter a research study?
To qualify and enter a research study, follow these steps:​​
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a. Screening Process: Participate in an initial assessment, which may include a review of your medical history, a physical exam, and lab tests to determine if you meet the study's eligibility criteria.
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b. Informed Consent: If you qualify, you will be provided with detailed information about the study and asked to sign an informed consent form.
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c.Enrollment: After consenting, you will be officially enrolled in the study and receive instructions on the next steps.
2. Why are drug studies conducted?
Drug studies are conducted to evaluate the safety, efficacy, and optimal dosing of new medications. These studies help to determine whether a new drug is effective in treating a specific condition and identify any potential side effects. The results from these studies are critical for gaining regulatory approval and ensuring that new treatments are safe and effective for patients.
3. Are research studies safe?
The safety of research studies is a top priority. Each study is carefully designed and reviewed by regulatory authorities and ethics committees to ensure it meets strict safety standards. Participants are closely monitored throughout the study, and any potential risks are thoroughly explained before enrollment. Our research team is always available to address any concerns and take immediate action if any issues arise.
4. Can I withdraw from a research study once I have started?
Yes, participation in a research study is completely voluntary. You can withdraw from the study at any time without any penalty or loss of benefits to which you are otherwise entitled. If you decide to withdraw, please inform the research team so they can ensure a safe and proper exit from the study.
5. What commitments are expected from research study participants?
As a research study participant, you are expected to:
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Attend Appointments: Show up for all scheduled study visits and follow-up appointments.
Follow Protocol: Adhere to the study procedures and instructions provided by the research team.
Report Information: Provide accurate and honest information about your health and any changes or side effects you experience during the study.
Stay in Communication: Maintain regular communication with the research team and report any issues or concerns promptly.
Complete Surveys/Diaries: Complete any required surveys, questionnaires, or diaries as part of the study protocol.
These commitments ensure the integrity of the study and contribute to its overall success.