Sponsor/CRO Info

Sponsor / CRO information

Experience, expertise and facility to meet the individual needs of each sponsor and research protocol

The MCRC Clinical research facility in Dayton location was carefully considered. Our facility was meticulously custom designed and constructed, employing all the knowledge of our experience. We are convinced that our 21 bed ward is “State of the Art”. We are equipped with the experience, expertise and the research unit facility to meet the individual needs of each sponsor and research protocol. Our facility is not a hospital, it is not a hotel, it is not an ICU, but it is a custom designed Clinical Research Center.

Record All Activity

We use a validated environmental monitoring system to record all activity of all pharmacy room temperatures, refrigerated / frozen drugs and samples stored within our research facility. Security Cameras are stratigically placed throughout our clinical research facility in Dayton, both inside and outside. 

Entry and Exit doors, including fire exits, are alarmed with audible sirens at all times to secure controlled access to and from the facility. Separation between volunteer inpatient and outpatient areas are strictly secured with locked doors accessible only by staff members with swipe-cards / push-button security codes.

Midwest Clinical Research Center is protected by a stand-by 40k watt natural gas generator. In the event of loss of Ohio Power & Light power to the building, the strong, but quiet generator automatically detects the loss and starts providing power to all essential portions of the facility. This includes: all the refrigerators, freezers, centrifuges, and security monitoring equipment. The natural gas supply allows the generator to work without interruption for an extended period of time.

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Clinical Studies Conducted

Midwest Clinical Research Center has been the site of over 150 clinical studies of the safety and efficacy and mechanisms of action of Phase I, II and III drugs as well as bioavailability and pharmacokinetic studies in normal subjects and in special populations. Numerous clinical studies have been successfully audited by sponsoring institution audit teams and by Food and Drug Administration Audit Teams.

Virtually all studies have been conducted under auspices of active IND applications and approximately 150 successful NDA’s have contained data generated by these studies, including:

Interested in partnering with the ERG network for your next study?

For more information, please visit our Sponsor/CRO website by clicking the button below:

STUDIES ARE ENROLLING NOW!

BUNION

Apply to participate in a study of an investigational pain medication following a bunion removal.

KNEE REPLACEMENT

Apply to participate in a study of an investigational pain medication following a knee replacement.

DEPRESSION

Take a self assessment to see if you qualify for a no cost mental health assessment with our medical team.