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Monday 7:30am - 3pm Tuesday 7:30am - 3pm Wednesday 7:30am - 3pm Thursday 7:30am - 3pm Friday 7:30am - 3pm

Fortrea Clinical Trials - Madison

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Madison, WI
Fortrea Clinical Trials - Madison

With clinical research units throughout the US and Europe, we enroll people to participate in the clinic.

02/19/2026

Your participation matters. Learn how to join a study by calling 1‑866‑429‑3700. 💚

02/17/2026

Before joining a study, it helps to know what to expect so you can make a confident, informed decision. Our team is ready to answer any questions—call 1‑866‑429‑3700 or visit fortreaclinicaltrials.com. 💚

02/14/2026

Share the love this Valentine's Day by participating in a clinical trial! ❤️

Learn more and browse available studies at FortreaClinicalTrials.com

02/10/2026

❌MYTH: You must have a condition to participate in a clinical trial.

✅FACT: Fortrea Clinical Trials conducts Phase 1 studies, for healthy participants. These studies help researchers determine the best dosing, timing and administration for a new treatment and also provide insights into how the drug reacts with the body.

02/06/2026

With our Refer-a-Friend program, you can score big no matter who wins the big game. 🏈💚
Earn up to $500 per qualified referral. Learn more at FortreaClinicalTrials.com

02/04/2026

Today is — a day dedicated to raising awareness about prevention, early detection, and treatment. 🧪

On this World Cancer Day, Fortrea honors the relentless spirit of those fighting cancer, remembers those we’ve lost, and recognizes the vital role of clinical research in advancing prevention and treatment.

01/29/2026

FAQ: What if I change my mind? 🤔

01/27/2026

Help advance medical research by spreading the word to others. 👥

To qualify, your friend must:

- Be new to Fortrea Clinical Trials or have not screened or participated in a clinical trial with Fortrea in the last 12 months
- Complete a screening appointment
- Fill out a Refer a Friend form at their screening appointment
- Qualify as a study participant

01/22/2026

Unlocking the future of medicine 🔓

When you participate in a clinical trial, you can help contribute to life-changing research!

01/19/2026

Celebrating the life and legacy of Martin Luther King Jr.

May his dream inspire our actions every day.

01/15/2026

Found a study you're interested in? Great!

Before entering a study, you must complete a couple of preliminary screenings with our team. This gives us the opportunity to talk to you and gather basic information that helps ensure your qualification for the study.

📞The first screening happens over the phone.
🩺This will be followed by an in-person screening at our clinic.

01/13/2026

❌MYTH: Once you join a clinical trial, you can't drop out if you change your mind.

✅ FACT: Participation in our clinical studies is always voluntary. You can withdraw your consent at any time. Once you’ve already started the clinical study, our doctors may need you to come back for a visit, just to check that the drug is out of your system.

Address

1910 Wright Street
Madison, WI
53704

Opening Hours

Monday	7:30am - 3pm
Tuesday	7:30am - 3pm
Wednesday	7:30am - 3pm
Thursday	7:30am - 3pm
Friday	7:30am - 3pm

Telephone

+16082105454

Website

https://www.fortreaclinicaltrials.com/clinical-locations/madison-wisconsin

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Our Story

Covance, with headquarters in Princeton, New Jersey, is one of the world’s largest and most comprehensive drug development companies. With the most comprehensive portfolio of preclinical, clinical development and commercialization services, Covance provides industry-leading services, the world’s largest central laboratory network, and a global team of clinical research and commercialization experts.

With clinical research units throughout the US and Europe, we enroll people to participate in clinical research studies to test new investigational products, and approved medications for new treatments. Covance Clinical Research Units are part of the Phase I/IIa drug development portion of Covance.

What We Do Covance carries out clinical research studies on behalf of the world's leading pharmaceutical and biotechnology organizations. As more drugs are being discovered, more people are needed to participate in clinical research studies.

Conduct of Studies Clinical research studies at Covance are conducted by a group of medically trained staff, including doctors and nurses, who monitor your safety during your participation.

Worldwide drug authorities have regulations to protect clinical research study participants and standards for how trials are conducted. It is required that participants are told what the purpose of the study is, what will happen during the study, risks and benefits of study participation, and background information on the investigational medication, including other studies involving the medication. An independent ethics board reviews the study, including all documents a participant will read and sign to make sure appropriate safeguards are in place. Study participation is always 100% voluntary from start to finish.

Types of Studies Clinical research studies are classified into four phases defined by worldwide authorities.

Phase I studies, including First-In-Human studies, are conducted in a small number of healthy participants to determine safety and tolerability. These studies test how drugs are absorbed into the body, as well as the amount of time the drug stays in the body. Safety of the drug and side effects are evaluated at varying dose levels. Additionally, interactions among multiple drugs, equivalence of a generic drug to a marketed drug and the effect of food on how the drug moves through the body may be studied.

Phase II studies also involve a limited number of participants and help provide an early indication for whether the drug shows promise in treating the condition for which it is being developed. These studies involve participants who have mild-to-moderate forms of the condition the drug is designed to treat, but who are otherwise healthy. Examples include:

People with diabetes, asthma and high blood pressure Healthy post menopausal women Healthy elderly

Phase III studies include thousands of participants with the disease or medical condition the drug is being developed to treat. These studies determine safety and effectiveness. They may compare the study drug to a current marketed treatment. Healthy individuals may participate in Phase III studies for smoking cessation, insomnia, vaccinations, weight loss, etc.

Phase IV studies involve further testing in large numbers of individuals after the product is released on the market.

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