Sponsors & CROs

Therapeutic Areas

  • IVD and medical device studies

  • Internal medicine

  • Cardiovascular

  • Metabolic / Obesity

  • Pulmonology

  • Pediatrics

  • Vaccines

  • Gastroenterology

  • Women's Health

  • Allergies

  • Dermatology

  • Oncology

Site Capabilities

At Altruistic Clinical Research we are committed to ensuring that our participants experience is the best it can be. To achieve this, we prepare our spaces so that they feel comfortable, safe, and at ease.

Waiting Area

Monitor Rooms

Coordinator Room

Exam Rooms

PK/Infusion Area

Pharmacy

Local Lab Access

Refrigerator

-20c Freezer

-80c Freezer

Dry Ice Access

Centrifuge/Refrigerated Centrifuge

EKG Machine

Crash Cart

Continuous Temperature Monitor

CLIA Certified

Double Locked Storage

Alarm System

Emergency Power Generator

Access to External Imaging

High Speed Internet

Site Information

At Altruistic Clinical Research we always look for diversity in our participants, as we know that this is very important to ensure that clinical trials demonstrate safety and effectiveness for everyone.

Patient Demographics

Male: 50%

Female: 50%

American Indian/Eskimo: 16%

Asian: 8%

Black/African American: 22%

Caucasian/White: 51%

Other: 3%

Hispanic/Latino: 62%

Non-Hispanic/Latino: 38%

Administration

Central IRB

Submission Timeline: 24 hrs

Contract Turnaround: 5 Business Days

Parallel Contractual Negotiations and Submissions

No FDA Audits

Quality Control

Data Entry

Partner with us

Experience the altruistic approach and advance your clinical study with patient-centered data!