top of page

About Us

TriPoint Research, LLC is a privately owned Site Management Organization specializing in Phases I – IV Clinical Trials since 2013. Currently operating in Houston, Texas, we provide our customers with the highest quality study services by centralizing functions for optimum results.

​

Our research background, work experience, commitment to delivering high quality results and extensive patient database gives us a competitive edge that attracts both Sponsors and CRO’s. â€‹

​

We strive to be an industry leader by negotiating fair budgets and contracts that lead to win-win relationships with our clients. 

 

We offer top quality services to Pharmaceutical, CRO and Biotechnology companies through the following methods listed below.

​

White File Folders
Centralized Management & Regulatory Functions

Our clinical management team regularly reviews all aspects of the clinical trials awarded to TriPoint Research.
 

Our Regulatory Department offers a central approach to document distribution & report maintenance while maintaining a presence at each site.  

 

All regulatory affairs are managed at a corporate level to ensure consistency throughout our organization.  Each regulatory coordinator is dedicated to a specific site and maintains all submissions, binders, and related documentation. 

Blue Keyboard
Study feasibility assessments & study start up procedures

The reputation of TriPoint Research partly depends on our ability to meet and exceed the contracted expectations of our customers.  As such, we provide study feasibility assessments for each trial presented to us.

​

TriPoint Research will always elect to use the central IRB delegated by the Sponsor / CRO. 

​

Business Meeting
Dedicated & Qualified Staff

TriPoint Research offers a staff of Principal & Sub Investigators with various specializations who are dedicated to the clinical research industry. 


Our CRCs, regulatory coordinators & CRAs have over 20 years combined industry experience and are required to complete rigorous training programs before actively participating in research projects.  

 

Trainings Include:

  • ICH / GCP / HIPAA – CITI Course

  • CRC Certification Exams

  • CCRA Certification Exams  

  • SOP Training Programs

  • CRA Pathway Program

CLINICAL RESEARCH EXPERIENCE

CARDIOLOGY

​

  • Hyperlipidemia

  • Hypercholesterolemia

  • Hypertension

  • Coronary Artery Disease

  • Peripheral Vascular Disease

BONE & MUSCULOSKELETAL

​

  • Lower Back Pain

  • Arthritis

  • Osteoarthritis

ENDOCRINOLOGY

​

  • Diabetes Mellitus Type I

  • Diabetes Mellitus Type II

  • Diabetic Neuropathy

  • Anemia

  • Obesity & Weight Loss

CENTRAL NERVOUS SYSTEM

​

  • Anxiety Disorder

  • Depression

  • Alzheimer's

ONCOLOGY

​

  • Dedifferentiated liposarcoma (DDLS) 

  • Breast 

  • Ovarian 

PULMONARY

​

  • Asthma

  • Pneumonia

  • COPD

  • Allergic Rhinitis

DERMATOLOGY

​

  • Atopic Dermatitis

  • Psoriasis 

bottom of page