Investigators

Investigators

Join Our Network

InFocus Clinical Research maintains a database of pre-qualified and proven investigator sites.

If you are interested in being considered for inclusion in our database and considered for future protocols, email Principal Investigator and Study Coordinator name, location, email and phone contact information and therapeutic experience to: info@InFocusClinical.com.

If you have a media kit or information packet, please forward it to:

InFocus Clinical Research
Attn: Investigator Development
205 Powell Place
Brentwood, TN 37027

Overview

InFocus Clinical Research has a proven and committed group of phase I sites pre-qualified to execute on your Phase I needs.

Additionally, InFocus Clinical Research specializes in providing clinical study expertise for the management of your Phase I trials. Regardless of your Phase I study type: first time in human, a dose tolerance study, a food effect study, a Pharmacokinetic (PK) study or a Pharmacodynamic (PD) study, our experienced staff can work with you to ensure:

  • Complete Site Development
  • SOP Development
  • Study Coordinator Orientation and Training
  • Quality Assurance Reviews
  • GCP Courses and Presentations
  • Mock FDA Inspections
  • FDA or Sponsor Preparatory Inspections
  • Urgent Care Service (On Call FDA Inspection Preparation)

All Quality Assurance Services include thorough interactive discussions, written report and recommendations for process improvement as well as follow up. Our Urgent Care Service caters to sites selected for FDA inspection and requiring STAT review of systems, data and preparatory support and recommendations.

STAFFING