to provide multiple, quality sites with one phone call
Ability to conduct Phase II through Phase IV
Large database of highly skilled, experienced
and enthusiastic Investigators
Dedicated, full time, and experienced
Physician Clinical Research Coordinators
Access to large patient populations with
Efficient and centralized contract and budget
Ability to conduct inpatient and outpatient
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.
Staffing with trained and experienced CRCs
Subject Recruitment Strategies
Independent protocol audits for QA and
Standard Operating Procedures (SOP)
development training for investigators and staff
On site facility assessment
Customized programs in:
with/interacting with Institutional Review Boards (IRB)
Understanding and complying with FDA, HHS and
Effective subject consent processes
Ethics/Protection of human
Current industry standards
(GCP, GLP, GMP)
Regulatory document preparation and maintenance