Diabetes Research Society

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   Diabetes Care
   DiabetOmics, LLC


  • Ability to provide multiple, quality sites with one phone call

  • Ability to conduct Phase II through Phase IV studies

  • Large database of highly skilled, experienced and enthusiastic Investigators

  • Dedicated, full time, and experienced Physician Clinical Research Coordinators

  • Access to large patient populations with cultural diversity

  • Efficient and centralized contract and budget resolution

  • Ability to conduct inpatient and outpatient studies

  • Strong working relationships with local and central IRBs and laboratories

  • Stable, effective and mutually beneficial working relationships with Investigative sites


      1.  We ensure timely and accurate regulatory board submission and data collection.

     2.  We provide access to a large patient study population.

     3.  We provide ongoing and effective communication between Site, Investigators and Customers.

Our experienced staff can be placed at any site to ensure high quality performance


All of the PIs in the DiaBaid network are highly experienced clinicians and researchers. We are not a clinical research training ground! In order to become a part of our network, a physician must demonstrate that they have successfully participated in at least 3 clinical studies.


Since we utilize our database to identify Subjects based on specific criteria of sponsors or other CROs, a significant amount of their time and resources are saved during the initial site identification, screening, and enrolment of clinical research subjects. 

Budgetary and contractual discussions are always centralized, thus minimizing lengthy negotiations. Upon agreement of a budget, a clinical trial agreement (CTA) can typically be executed within a day or two.

Trial Management

Staffing with trained and experienced CRCs

  • Subject Recruitment Strategies
  • Data Management
  • Independent protocol audits for QA and training purposes
  • Budget negotiations

Site Management

  • Site specific Standard Operating Procedures (SOP)
  • Quality Assurance
  • Audit Services  


  • On site development training for investigators and staff
  • On site facility assessment
  • Customized programs in:
    • Working with/interacting with Institutional Review Boards (IRB)
    • Understanding and complying with FDA, HHS and HIPAA regulations
    • Effective subject consent processes
    • Ethics/Protection of human subjects
    • Current industry standards (GCP, GLP, GMP)
    • Regulatory document preparation and maintenance