We at Delta Research Partners realize that you have many clinical research sites available to choose from. We hope that you will consider selecting us to partner with in meeting your clinical trial needs. We recognize the benefits of providing you with accurate data in a timely fashion while providing patient services in a quality manner.
I promise that we will provide the following:
- CTA/Budgets and Contracts will be completed expeditiously. We have no bureaucracy within our organization and are able to complete documents quickly. We guarantee to return all study documents within 48-72 hours.
- We utilize the IRB of your choice or a central IRB for efficiency. We do not use a Local IRB.
- We welcome you to visit our site any time at your convenience. We have no required “check-in” or “check-out” times. Sponsors/Monitors will always have easy access to our facilities to monitor and review their study’s progress.
- After many years (since 2003) in conducting clinical trials we have had several FDA audits but never been issued a Form 483.
- We invest in the training, education and development of our Research Coordinators. We also recognize them to be our largest asset. Our ability to conduct successful trials is based on their skills and attention to details.
We look forward to partnering with you and we assure you that your visit to Northeast Louisiana will be an enjoyable one.
Raj Bhandari, M.D., P.I.