About Us

Your Partner in Clinical Research and Healthcare Solutions

About PRX Research: Advancing Medical Innovation in North Texas

PRX Research is a leading clinical research organization in North Texas, dedicated to accelerating biomedical discoveries into real-world healthcare solutions. Our multidisciplinary team of experts utilizes cutting-edge technologies and collaborative partnerships to drive medical advancements and improve patient outcomes.

Our Advanced Research Facility: A 202-Bed Hospital Setting

Located within a state-of-the-art 202-bed hospital, PRX Research provides a comprehensive environment for clinical trials and medical research. Our facility offers 24-hour emergency care, critical care, and a full range of diagnostic and treatment services, ensuring patient safety and seamless research execution.
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Streamlined Research Processes: Rapid IRB and Regulatory Approvals

PRX Research accelerates clinical trials with a centralized IRB, ensuring rapid regulatory, contract, and budget approvals. Our efficient recruitment processes and inpatient/outpatient capabilities enable timely and effective research execution.
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Expert Team and Collaborative Research for Meaningful Results

Our experienced multidisciplinary team collaborates with researchers and partners to translate biomedical discoveries into impactful healthcare solutions. We leverage our expertise and state of the art facilities to deliver research results that improve patient lives.
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Innovative Clinical Trials

Pioneering Patient-Centric Care and Advancing Medical Science for Future Generations

We are passionate about providing patients with access to innovative treatments and improving the health of our community. With a focus on patient-centric care and scientific excellence, we conduct clinical trials across a wide range of therapeutic areas. Join us in shaping the future of medicine and transforming healthcare for generations to come.

What Happens During a Clinical Trial?

Participating in a Clinical Trial:
What to Expect at PRX Research

At PRX Research, we prioritize patient safety and informed participation in clinical trials. Here’s an overview of the process:

Our team will conduct a pre-screening to determine if you meet the eligibility criteria for the study. This may involve reviewing your medical history and discussing your current health status.

Before enrolling in a clinical trial, you’ll receive detailed information about the study, including its purpose, procedures, risks, and benefits. You’ll have the opportunity to ask questions and discuss any concerns with our research team. Once you fully understand the study and agree to participate, you’ll be asked to sign an informed consent form.
You will receive a copy of the informed consent form, which you can keep for future reference. It’s important to remember that informed consent is an ongoing process. You are encouraged to ask questions about your participation at any point during the study, even after you have signed the form. Our research team will also keep you updated about any new information that might affect your willingness to continue participating.

During the screening visit, we’ll conduct a thorough assessment to confirm your eligibility for the trial. This may include a physical exam, medical tests, and a review of your medical records.

Once enrolled, you’ll actively participate in the clinical trial according to the study protocol. Our research team will closely monitor your health, provide ongoing support, and answer any questions you may have throughout the process. Remember, your participation is voluntary, and you can withdraw from the study at any time.

Upon completion of the clinical trial, we’ll provide you with information about the study results and any potential next steps. Your contribution to medical research is greatly appreciated!