View Our Locations

614-501-6164

Clinical Trials and Medical Research
Studies in Columbus Ohio

Sponsors

Aventiv Research has several key strengths that enable us to provide outstanding service to our sponsors:

  • We provide outpatient services in a modern 3,000 square foot clinical research facility.
  • Aventiv Research utilizes a central IRB with a 24-48 hour turnaround time for regulatory, budgets and contacts.
  • A comprehensive volunteer tracking system.
  • Experienced staff who are CPR and IATA certified.

Our Clinical Research Facility includes:

  • IATA and CLIA certified
  • -80 degree freezer
  • -20 degree freezer
  • Overnight visits
  • 10 patient beds
  • 10 patient exam rooms

Read More

Staff Credentials

Dr. Samir Arora is Board Certified in Family Medicine as well as CPI certified. He has been doing research for over ten years.

All staff are CPR and IATA certified. The experience level of our coordinators ranges from three to fifteen years, with an average of 10.

Read More

Enrollment Capacity

We use utilize Clinical Conductor, a Clinical Trial database system that lets us track and monitor all of our patients. Our database consists of over 12,000 patients and is continuously growing. Aventiv Research is known as one of the leading enrolling research facilities in Ohio. We pride ourselves in enrolling quality volunteers at a rapid rate.

Quality Assurance Department

  • Standard operating procedures annually reviewed and updated.
  • Internal auditing including tracking of error rates, query rates and interventions.
  • Patient surveys given at end of visits.
  • Monthly staff meetings to review studies and educational material.

Volunteer Demographics

  • Standard operating procedures annually reviewed and updated.
  • Internal auditing including tracking of error rates, query rates and interventions.
  • Patient surveys given at end of visits.
  • Monthly staff meetings to review studies and educational material.

IRB Central

Aventiv Research utilizes a central IRB. Our turnaround time for regulatory, budgets and contacts is 24-48 hours. We do not have to have a contract signed before we can proceed with regulatory documents.

Michelle LaPage

Director of Business Development

Having been in the industry since 1989, I have a base of knowledge to help CROs and Sponsors to plug into the site services Aventiv offers. I welcome the opportunity to assist with new studies. Please contact me as follows:

Aventiv Research, Inc. (formerly Columbus Clinical Research)
Cell: 612-281-7084
Desk Phone: 763-767-4409
Email: mlapage@aventivresearch.com