GFS National Research Center Corp

Informed Participation

To participate in any study, patients must:

• Meet the protocol’s inclusion and exclusion criteria.
• Sign an IRB-approved informed consent form.
• Provide truthful information during evaluation.

Pre-Study Transparency

Before enrolling, each patient receives information about:

• The study objective.
• Risks and benefits.
• The expected duration.
• Participant rights.
• The freedom to withdraw at any time without penalty.

No procedure begins without signed consent.

Participant Rights

• Be treated respectfully.
• Leave the study at any point.
• Request additional study information.
• Keep all personal data confidential.

Compensation & Safety

• Financial compensation for time and travel when applicable.
• Medical care in the event of a study-related adverse event.
• Details about benefits are noted in each protocol’s informed consent.

Study Changes

The Clinic may cancel or modify a study when required by the sponsor, for safety reasons, or upon request from the ethics committee or regulatory authorities.

Limitation of Liability

• Not responsible for misuse of data after lawful delivery.
• Not responsible for adverse events unrelated to study procedures.
• Not responsible for false information provided by participants.

Legal Framework

These terms are governed by the laws of the State of Florida within the United States of America (USA).

Contact

GFS National Research Center Corp

Email: info@gfsnationalresearch.com

Phone: 786-637-2952

Address: 10631 N Kendall Dr, Suite 125, Miami, Florida 33176