Why It Matters

Clinical trials are designed to:

• Evaluate the safety and efficacy of investigational treatments

• Improve the quality of patient care

• Advance treatment options for chronic and life-threatening conditions

• Support regulatory approval of new therapies

The data collected from these trials helps researchers, regulatory agencies (like the FDA), and healthcare providers bring life-saving treatments to the public.

Who Can Participate?

We conduct studies involving diverse adult populations, including healthy volunteers and individuals living with conditions such as:

• Diabetes

• Pain disorders

• Infectious diseases

• Women’s health conditions

• Cardiovascular risks

• Mental health and more

Each study has specific eligibility requirements. Our team will guide you through a simple pre-screening process to determine which studies you may qualify for.

What to Expect as a Participant

Clinical trial participation typically includes:

1. Pre-screening interview (by phone or online)

2. On-site evaluation with free lab work and medical assessment

3. Informed consent — we’ll explain everything clearly

4. Participation in the study protocol

5. Follow-up visits, monitoring, and support

You’ll never be asked to pay for any procedure related to the study, and compensation may be available. No insurance is required, and free transportation may be provided for qualified participants.

Your Rights and Safety

All clinical trials conducted at Navia’s Clinical Research are:

• Overseen by licensed medical professionals

• Reviewed and approved by Institutional Review Boards (IRBs)

• Compliant with FDA and Good Clinical Practice (GCP) guidelines

We prioritize your safety, privacy, and comfort at every stage of the process.