Participate In A Medical Research Study Today!
Benefits of Participation
When you participate in a research study:
- Assist in the development of new medications and combinations (ie. allergy, respiratory, diabetes, growth, skin conditions, COPD, and cold/flu/pneumonia)
- Improving existing treatments
- Potential benefits to you as a participant, including study related care and testing
- Potential participant financial benefits, including compensation for time and travel
When you volunteer to participate in a study, you will be contacted by a study coordinator and will be asked to review specific study information as contained in the informed consent. You will have an opportunity to read the informed consent, discuss the contents with family members and Primary Care Physician, and ask questions of the Principal Investigator and/or Research Coordinator. Once the informed consent has been signed and you choose to volunteer, you will be screened for study specific inclusion and exclusion criteria, study procedures such as vital signs, medical history, and preliminary evaluations. Please note you can ask questions at any time and should you choose to withdraw your consent (drop out of the study) it is your right to do so. All aspects of the study, including rights, responsibilities, compensation for your time and travel, physical exams, lab work, and other assessments will be discussed in full detail during the consent process.
View/Download – Medical Release
If you are interested in learning more about current research studies and participation opportunities, please complete the form below. Upon receiving your information, we’ll contact you regarding research opportunities.
