For Sponsors & CROs

Operationally excellent research sites, built for sponsors

Trusted by sponsors for delivering reliable, diverse, and high-quality clinical research across Metro Detroit.

Start feasibility

Download capabilities

27k+Patients in network

11+Partner clinics

48–72hFeasibility turnaround

GCPFully compliant

Site capabilities

People · Process · Tech

GCP-trained coordinators & PIs

Regulatory startup & IRB submissions

On-site processing (centrifuge, −80°C storage)

ECG, vitals, spirometry, phlebotomy

Remote eSource & eReg systems

IATA-certified specimen handling

Source document creation & QC

Dedicated recruitment coordination

Therapeutic focus

Core strengths

Internal Medicine & Primary Care

Respiratory / Pulmonology

Ophthalmology

Cardiology

Neurology & Psychiatry

Dermatology

Endocrinology & Metabolism

Pediatrics

Infectious Disease

Nephrology

Gastroenterology

Allergy & Immunology

Quality & compliance

SOP-driven operations

100% ICH-GCP compliance; central IRB capable

Calibrated equipment & temperature-controlled storage

SOP-based regulatory workflows and monitoring readiness

Rapid site startup — 48–72h feasibility turnaround

How engagement works

One dedicated point of contact

Feasibility

Send your protocol synopsis; get a realistic enrollment read within 48–72 hours.

Startup

Centralized contracts, budgets, and IRB submissions run in parallel — not in sequence.

Enrollment

Physician panels refer from established patient populations — you see progress early.

Close-out

Clean data, resolved queries, and a team that answers the phone — start to finish.

Have a protocol in mind?

Send us the basics and get a realistic feasibility read from our team within 48–72 hours.

Request a feasibility review