Experience. Quality. Productivity. Excellence.

Resources at your fingertips

Remington-Davis is conveniently located close to a major international airport and downtown Columbus, Ohio. In addition to on-site clinical facilities, coordinators have immediate access to the following:

We have the following resources to ensure Quality data and that your monitors can be as efficient as possible while on site:

• Internal Quality Assurance Program 
• 4 dedicated monitoring rooms
• Wireless high speed internet (hard-wired available, if necessary)
• GCP/ICH training documentation
• IATA training documentation
• EDC/RDC training documentation

Why we are Different:

• Internal Quality Assurance program ensures quality data and fewer queries.
• Dedicated, professional research site
• Focus on clinically and logistically complex trials
• Conduct both inpatient and outpatient trials
• Full time Regulatory Coordinator ensures rapid study start up and turn-around time on essential documents. 
• Coordinators focus on recruitment, enrollment and evaluability
• Investigators associate with Remington-Davis because of our experience, professionalism and reputation, not exclusive contracts
• Large database of interested volunteers

Study Experience:

• Excellence since 1992, evidenced by repeat business and solid relationships with major pharmaceutical sponsors and CRO’s
• Over 350 studies conducted in 18 Therapeutic Areas
• Thousands of evaluable patients enrolled

Service:

• Dedicated, in-house coordinators ENROLL
• Full time regulatory team ENSURES QUALITY DATA
• Knowledgeable and friendly support staff make COMMUNICATION EASY