Delivering Exceptional Value to Sponsors & CROs

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At Focus Clinical Research, we strive to deliver exceptional value to our sponsors and CROs. Our team of physicians with diverse specialties is dedicated to conducting comprehensive research studies from Phase II to IV with the utmost excellence. We take immense pride in providing a highly skilled research team with a proven track record of success in clinical trials. Our primary goal is to achieve all objectives our sponsors and CROs set, including delivering high-quality data and efficiently surpassing enrollment targets.

The key to our success lies in the expertise and diversity of our corporate team. This knowledgeable group is fully involved in every aspect of our clinical operations to ensure we meet and exceed our partners’ expectations in every

Performance

  • Swift and effective initiation
  • Assurance of screening shortly after Site Activation
  • Assurance of meeting enrollment limits
  • Quality assurance in real-time
  • Automated updates of EDC from e-Source in real-time

Multi-Specialty Site

  • Dermatology
  • Gastroenterology
  • General Medicine
  • Infectious Disease
  • Internal Medicine
  • Neurology
  • Ophthalmology
  • Pulmonology
  • Urology
  • Vaccines
  • Women's Health
  • Dermatology
  • Gastroenterology
  • General Medicine
  • Infectious Disease
  • Internal Medicine

Building Trust with Study Participants

If you are looking to make a valuable contribution to medical research and improve your health and future generations, you have the opportunity to participate in one of our clinical studies here at Focus Clinical Research. We are excited to offer a range of new and ongoing studies, and you can quickly join us through our website. If you require any assistance with the registration process, please feel free to call us at any time, and a member of our team will be happy to help.

Operational Capabilities

Key Capabilities Key Benefits
Electronic Source
  • Integrate data automatically using study EDC
  • Monitor remotely
  • Compliant with 21 CFE Part 11 regulations
  • Ensure real-time Quality Assurance with embedded edit checks
Stipend Cards
  • Automated processing of stipend payments that ensures compliance with ICF guidelines
  • Enhanced retention of subjects
Experienced Research Staff
  • Research experience from Phase 1 to 4
  • Staff members have an average of 4.5 years of experience
  • Positive reviews and awards for quality from different Sponsors and CROs drive on-time study startup
Six Sigma Project Management
  • Drives on-time study startup
  • Customized solutions applied to each study vs. standard fit-in-the-box solutions from competitors
  • Check-n-balance approach to maintain high quality and maximize study efficiency

Enhancing
Recruitment

  • The process of pre-screening starts at Site Selection, unlike most sites that wait for Site Activation.
  • Integrate text and email marketing with real-time automated subject enrollment for a targeted study.
  • Large social media presence with highly effective digital marketing capabilities
  • Automated HIPPA release and appointment reminders/confirmations
  • Sponsors and CROs have received several recruitment awards for exceeding their enrollment commitments.