Advancing Medicine Through Clinical Research
Transforming lives by connecting patients to innovative therapies.
Transforming lives by connecting patients to innovative therapies.
Our mission is to advance medical solutions that improve health outcomes by conducting responsible, ethically guided clinical research. We are committed to supporting studies that address critical health challenges and benefit diverse communities locally and globally.
We are guided by a strong commitment to scientific integrity, ethical responsibility, and respect for every individual who participates in clinical research. Our work is grounded in transparency, regulatory compliance, and meaningful collaboration with investigators, sponsors, and participants to ensure research is conducted safely, responsibly, and with purpose.

During pre-screening, our research team gathers basic information to determine whether a study may be a good fit for you. This may include questions about your medical history, current condition, and eligibility requirements.

Before any study procedures begin, you will review and sign an informed consent form. This document explains the study’s purpose, procedures, potential risks and benefits, and your rights as a participant. Our team will answer all questions to ensure you fully understand the study.

At the screening visit, study-specific evaluations are performed to confirm eligibility. These may include medical exams, laboratory tests, imaging, or questionnaires, depending on the study protocol.

If you meet all eligibility criteria, you may be enrolled in the study. Enrollment confirms your participation and allows study activities to begin according to the approved research plan.

Throughout the study, you will attend scheduled follow-up visits. During these visits, our team monitors your health, collects study data, and ensures your safety while you receive study-related care.

At the end of the study, final evaluations are completed, and your participation concludes. Our team will review next steps with you and answer any remaining questions. Participation is always voluntary, and you may withdraw at any time.


All studies are conducted in accordance with FDA regulations and Institutional Review Board (IRB) approval.
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Regis Clinical Research is an independent clinical research organization dedicated to advancing medical science through high-quality, ethical, and patient-centered clinical trials. The company partners with pharmaceutical, biotechnology, and medical device sponsors to conduct clinical research that supports the development of innovative therapies and diagnostics while maintaining the highest regulatory and scientific standards.
Regis Clinical Research conducts clinical trials and translational research across multiple therapeutic areas, evaluating the safety, effectiveness, and real-world application of investigational drugs, biologics, medical devices, and diagnostic tools. The research is conducted in compliance with ICH-GCP guidelines and applicable regulatory requirements, with a strong focus on data integrity, patient safety, and meaningful clinical outcomes.
Regis Clinical Research’s work benefits patients, by providing access to innovative therapies and advancing future treatment options; healthcare professionals, by contributing clinical data that informs evidence-based care; and industry sponsors and research partners, by delivering reliable, high-quality clinical data that supports product development, regulatory submissions, and scientific advancement.

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