Our Phase II & III Capabilities

Many of our sites have participated in research for 10+ years. Our partnerships provide access to CA residents throughout the State with nearly 20 partnerships in over 50+ locations. We help provide access to a diverse patient population, including minority groups that otherwise go unrepresented in research. 

Rapid Start

  • Central IRB.
  • Contract and budget response within 48 hours.
  • Regulatory documents completed in parallel.
  • Often able to complete start-up within 2 weeks.
  • Dedicated Call Center team to assist with enrolling.

Capabilities

  • FibroScans, ultrasounds, X-rays, PBMC, local labs, and much more available at many locations. 
  • Nearby access to liver biopsy, MRI-PDFF, DEXA, CT-Scans, and much more.  
  • Efficient prescreening process.
  • Experience with telemedicine, virtual, and hybrid trials.

Quality Control

  • Our Internal quality team provides QC on all ICF and critical documents.
  • eRegulatory and eSource offer increased quality and efficiency.
  • eDocuments available for sponsor review 24/7.

Our Therapeutic Areas

Allergy and Immunology

Cardiology

Dermatology

Family Medicine

Gastroenterology

Infectious Disease

Internal Medicine and Vaccines

Nephrology

Neurology

Obstetrics and
Gynecology

Oncology

Pediatrics

Ophthalmology

Retina

Rheumatology

Urology

Our Diversity Data

* We are actively working on further engaging and bringing clinical trials to this unrepresented minority group.