MediSphere Medical Research Center

MediSphere Medical Research Center Medisphere Conducts Phase II, III And IV Regulated Clinical Trials for the Medical Industry.

MediSphere is an independent, dedicated clinical research center which conducts Phase II, III and IV clinical research for pharmaceutical, biotechnology, nutritional, and medical device industries. Founded in 1992, MediSphere has participated in more than 600 national and multinational clinical trials. MediSphere has more than 25,000 active patient files in Evansville, IN, the major city in the Tri-State area. The Tri-State, with a population of 1.2 million, is composed of 11 counties in Southwest Indiana, 9 in Western Kentucky and 10 in Southeast Illinois. MediSphere is a member of the Alliance for Multispecialty Research (AMR), an independent Site Alliance (ISA) of established, geographically diverse, professional clinical research sites. This not-for-profit support organization is composed of 15 multi-therapeutic, highly experienced research centers across the United States. FDA Audits in October 1999 and May 2001 showed no deficiencies and no 483's issued.

12/23/2025

Merry Christmas and Happy New Year. Thank you to all who take part in clinical research trials-your participation brings hope, innovation, and better care for future generations.

12/12/2025

Enrolling for Paid Clinical Research Studies Phase III and IV.
Participation is voluntary.
All studies are conducted by experienced professionals.
Call Now 812-471-4110 to see if you qualify.

Medisphere Conducts Phase II, III And IV Regulated Clinical Trials for the Medical Industry.

12/10/2025

Get your blood pressure checked at least once a year and understand what the numbers mean. Severe high blood pressure combined with symptoms such as chest pain or trouble speaking may be a hypertensive emergency, according to the new high blood pressure guideline, and you should call 911 immediately.

11/26/2025
Your safety comes first.Every study at Medisphere Research follows strict FDA and IRB-approved guidelines to keep partic...
11/19/2025

Your safety comes first.
Every study at Medisphere Research follows strict FDA and IRB-approved guidelines to keep participants protected, monitored, and supported throughout the entire process.
SAFE. COMPASSIONATE. RESEARCH YOU CAN TRUST.

Today is World Diabetes Day 💙We’re proud to be part of the journey toward better treatments and brighter futures for tho...
11/14/2025

Today is World Diabetes Day 💙
We’re proud to be part of the journey toward better treatments and brighter futures for those living with diabetes.

11/10/2025

Struggling to manage Type 2 Diabetes and weight?

Join our clinical study at MediSphere Medical Research and help advance new treatments - while receiving expert care close to home.

Limited space available for this study. Call today! 812-471-4110

11/03/2025

Get Paid Today for Participating in Our Clinical Trials. Call 812-471-4110 to see if you qualify.

Address

4411 Washington Avenue Suite 147
Evansville, IN
47714

Opening Hours

Monday 7:30am - 5pm
Tuesday 7:30am - 5pm
Wednesday 7:30am - 5pm
Thursday 7:30am - 5pm
Friday 7:30am - 5pm

Telephone

+18124714110

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Our Story

MediSphere is an independent, dedicated clinical research center which conducts Phase II, III and IV clinical research for pharmaceutical, biotechnology, nutritional, and medical device industries. Established in 1992, MediSphere has participated in more than 750 national and multinational clinical trials. MediSphere has more than 25,000 active patient files in Evansville, IN, the major city in the Tri-State area. The Tri-State, with a population of 1.2 million, is composed of 11 counties in Southwest Indiana, 9 in Western Kentucky and 10 in Southeast Illinois. MediSphere is a member of the Alliance for Multispecialty Research (AMR), an independent Site Alliance (ISA) of established, geographically diverse, professional clinical research sites. This not-for-profit support organization is composed of 15 multi-therapeutic, highly experienced research centers across the United States. FDA Audits in October 1999 and May 2001 showed no deficiencies and no 483's issued.

It is our mission to provide reliable clinical data to help advance new medical treatments. We have become one of the most reputable clinical research centers in the area. Leading and upcoming pharmaceutical companies have trusted and allowed us to be a part of their compound development and clinical studies to be conducted in a most professional and ethical manner. Through this process, we are granted the opportunity to help the people of our community to improve their quality of life in maintaining dignity and respect as well as Health Care Providers and the general public in having access to promising new medical treatment and technologies.