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In order to assure you are getting the test your physician requires, it is important that you have the order. Please contact your physician to obtain an order so you can be scheduled properly.

 

Aultman Wait Times

Choose Immediate Care for colds/flu, sprains/strains and other minor injury/illness.


Go to the ER for major concerns and trauma. Call 911 for chest pain and stroke symptoms.

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Location Finder

Here's your guide to finding any of the facilities in the Aultman family of health services, including maps and contacts. 

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Need a Doctor?

Aultman's network of providers is committed to high-quality patient care.

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Schedule an Appointment

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You can help support and enhance services, and in turn, help patients and their families who benefit from care received at Aultman.

Research Oversight

Only treatments that show great promise and have been tested thoroughly in the lab are studied in clinical trials.

Protecting the safety of the individuals who take part in clinical trials is a high priority. Each trial has scientific oversight and patients also have rights that help protect them.

Institutional Review Board

Institutional Review Boards (IRBs) are independent committees that oversee the conduct and safety of a clinical trial - all studies are appointed an IRB.  The IRB reviews the trial's protocol before the study begins and continually monitors the study to ensure safety and that patients' rights are protected. Aultman has a local IRB committee that is comprised of doctors, nurses, pharmacists and community members.

Data Safety Monitoring Board

Most clinical trials are required to have a Data and Safety Monitoring Board (DSMB). A DSMB's role is to regularly review data collected from a clinical trial to make sure there are no safety problems or differences in results among different groups. The DSMB makes decisions whether or not to continue a trial or stop it. For example, some trials are stopped early if benefits from a strategy or treatment are obvious. That way, participants can be granted access to the new strategy sooner. 

Office for Human Research Protections and Food and Drug Administration 

In the United States, the Office of human Research Protections (OHRP) and/or the Food ad Drug Administration (FDA) oversee clinical trials. The FDA reviews applications for new medicines and devices before any testing on humans is done.

location icon

Location Finder

Here's your guide to finding any of the facilities in the Aultman family of health services, including maps and contacts. 

symptom checker icon

Need a Doctor?

Aultman's network of providers is committed to high-quality patient care.

calendar icon

Schedule an Appointment

Click below to complete an online form. 

 

donation icon

Donate Today

You can help support and enhance services, and in turn, help patients and their families who benefit from care received at Aultman.

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