Vilo Research Group
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Phase I–IV · Biospecimen · Diagnostics · IVD

Clinical Research Network in Houston for Sponsors, CROs, and Diagnostic Programs

Phase I–IV trials, biospecimen programs, and IVD support with access to diverse populations, bilingual recruitment, and 5-site coverage across Greater Houston.

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Pharma TrialsSponsor & CRO-led Phase I–IV clinical studies with full-site execution.
Biospecimen ProgramsProtocol-aligned collection workflows with compliant processing and chain-of-custody.
IVD & DiagnosticsClinical specimen acquisition and operational support for diagnostic and validation programs.
Built for Sponsors, CROs, and Diagnostic Companies

Fast feasibility. Reliable enrollment. Collection-ready operations.

VRG is designed to support pharma clinical trials, biospecimen programs, and diagnostic research requiring responsive feasibility, strong participant access, and reliable execution across Greater Houston.

  • Sponsor and CRO-led pharma trial support
  • Biospecimen programs and protocol-aligned workflows
  • IVD and diagnostic study support
  • Bilingual prescreening and scheduling
Operational Scale & Participant Access
Network Strength

VRG at a Glance

7

PIs in Network

~10,000

Study Database

~325

Monthly Visits

2016

Est. Founded

5

Locations

EN/ES

Languages

Capabilities

Clinical Research Capabilities

VRG supports a broad range of sponsor-led clinical development programs with operational discipline and community reach.

Phase I–IV Clinical Trials

Support for interventional and observational studies across multiple therapeutic areas.

Biospecimen Collection Programs

High-volume collection with compliant chain-of-custody and processing workflows.

IVD and Diagnostic Validation

Clinical specimen acquisition and validation support for diagnostic assays.

Medical Devices

Clinical site support for device studies and technology validation programs.

Bilingual Participant Recruitment

Physician referrals, community outreach, digital and database recontact.

Feasibility Response within 48 Hours

Structured protocol review for sponsors and CROs within 48 hours.

Why Vilo

Why Sponsors and CROs Choose VRG

Operational discipline, community trust, and bilingual engagement designed to improve participant access, clinical trial execution, and specimen collection readiness.

Diverse Population Access

Strong access to Hispanic and underserved communities (70%+ Hispanic participant base).

Bilingual Operations

English/Spanish research staff across recruitment, prescreening, scheduling, and follow-up.

Multi-Site Network

5 locations across Houston and Katy with coordinated participant workflows.

Diagnostic & Biospecimen Expertise

BSL-2 lab, -80°C storage, barcode chain-of-custody, and validated cold-chain shipping.

Therapeutic Areas

Therapeutic Areas of Experience

Clinical research experience across multiple disease areas with specialized investigator expertise and community-based participant access.

Infectious Disease & Respiratory

Vaccines

Women's Health & Gynecology

Gastroenterology

Diagnostics & IVD

Biospecimen Programs

Cardiovascular & Metabolic

Musculoskeletal & Pain

Infrastructure

Site Infrastructure & Compliance

Purpose-built infrastructure for clinical trial execution, biospecimen collection, and diagnostic study support.

BSL-2 Laboratory

Certified Biosafety Level 2 facility for specimen processing and storage.

−80°C Ultra-Cold Storage

Long-term specimen preservation for demanding biospecimen protocols.

Cold-Chain Shipping

Validated dry ice, wet ice, and temperature-monitored courier shipping.

Barcode Chain-of-Custody

End-to-end traceability from collection through final delivery.

IRB & GCP Compliant

All protocols managed under active IRB oversight and GCP training.

HIPAA Compliant

Secure data management with full participant privacy protections.

149+ Combined Clinical Studies
Investigator Network

Principal Investigator Network

Board-certified investigators across multiple therapeutic areas supporting clinical trial execution, biospecimen programs, and diagnostic research.

Jorge Mendez, FMG, RN

Jorge Mendez, FMG, RN

Clinical Research

Founder & CEO — Clinical Research Investigator

58+ studies
Dr. Luis Zepeda

Dr. Luis Zepeda

Family Medicine

Board-Certified Family Medicine

42+ studies
Dr. Nelson Uzquiano

Dr. Nelson Uzquiano

Obstetrics & Gynecology

Board-Certified OB-GYN

21+ studies
Dr. Harry Ojeas

Dr. Harry Ojeas

Gastroenterology

Board-Certified Gastroenterology

12+ studies
Dr. Elvis Massip

Dr. Elvis Massip

Family Medicine

Board-Certified Family Medicine

6+ studies
Dr. Andres Vasquez

Dr. Andres Vasquez

Cardiology

Board-Certified Cardiology

5+ studies
Dr. Wigberto Soto

Dr. Wigberto Soto

Obstetrics & Gynecology

Board-Certified OB-GYN

5+ studies
Research Experience

Active & Recent Research Experience

A selection of clinical trials and research programs supported by VRG across Greater Houston.

Active

Knee Osteoarthritis

Phase 3 study for chronic knee pain (HOPE4OA). Sponsor-led clinical research program.

MusculoskeletalHouston / Katy
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Research Experience

Women's Health

Investigational study for vulvovaginal candidiasis (VVC) symptom relief validation.

GynecologyHouston / Katy
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Active

Diabetes / Metabolic

Next-generation studies for Type 2 diabetes and metabolic health monitoring.

MetabolicHouston / Katy
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Active

Respiratory & Vaccines

RSV, flu, and respiratory illness prevention studies for diverse populations.

Infectious DiseaseHouston / Katy
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Recent

Healthy Volunteers

Biospecimen collection opportunities for longitudinal health tracking.

Healthy VolunteersHouston / Katy
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Active

Fatty Liver / NASH

Clinical trials for fatty liver disease and NASH with specialized liver monitoring.

GastroenterologyHouston / Katy
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Sponsors, CROs, & IVD Companies

Evaluate VRG for Your Next Study

Submit your protocol or study concept. Our team will assess feasibility, population fit, and operational readiness within 48 hours.

Request Feasibility ReviewExplore Capabilities