Terms & Conditions
State of Florida, United States of America
This document sets forth the terms and conditions under which GFS National Research Center Corp (the “Clinic”) provides clinical research services and enrollment in pharmaceutical studies. By using our services or requesting participation, you accept these terms.
The Clinic conducts pharmaceutical studies, including:
All studies receive Institutional Review Board (IRB) approval and comply with applicable federal and state regulations.
To be considered for a study, participants must:
The Clinic reserves the right to accept or decline participants based on medical or study-specific considerations.
GFS National Research Center Corp commits to protecting personal and medical information in accordance with HIPAA and applicable laws in Florida. We use data only for study purposes, anonymize or code records as required, and share information solely with the study sponsor, authorized regulatory bodies, or the ethics committee when necessary.
Before joining any study, participants receive information about the study’s objective, duration, methodology, risks, potential benefits, medical procedures, participant rights, and safety measures. No procedure occurs without a signed IRB-approved informed consent.
Participants acknowledge that pharmaceutical studies may carry risks, including side effects or adverse events. Benefits cannot be guaranteed, and some effects may be unknown due to the experimental nature of the investigational product. The Clinic applies all required safety measures per regulatory standards.
Compensation may be provided for time and participation, as well as transportation expenses. Specific payment details are included in each study’s informed consent form. In case of study-related adverse events, the Clinic follows sponsor and regulatory guidance.
The Clinic may cancel, suspend, or modify a study if requested by the sponsor, the ethics committee (IRB), FDA, or other regulatory authorities, or when safety concerns arise that affect participants.
The Clinic is not liable for adverse events unrelated to the study, false or incomplete information provided by participants, failure to follow protocol instructions, or misuse of shared data by authorized third parties.
These terms are governed by the laws of the State of Florida and applicable federal regulations in the United States concerning clinical research.
GFS National Research Center Corp
State of Florida, USA
Email: info@gfsnationalresearch.com
Phone: 786-637-2952
Address: 10631 N Kendall Dr, Suite 125, Miami, Florida 33176
We can also produce supporting documents such as privacy notices, tailored informed consents, recruitment formats, patient notices, and internal regulations.
Updated to describe how we collect, store, and share personal and medical data in line with HIPAA and Florida requirements.
Clear, IRB-approved consents per protocol covering risks, benefits, procedures, and participant rights.
Includes call scripts, screening forms, and visit guides to document prospective subjects.
Notices reinforce safety, privacy, and expected conduct during study participation.
Contact our regulatory team at info@gfsnationalresearch.com to request these documents.
