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CNS Veritas offers sponsors a clinically rigorous, operationally reliable research site with experienced principal investigators and a dedicated team committed to delivering quality data — on time, every time.

FOR SPONSORS

A clinical trial site built for precision, performanceand partnership.

What sets us apart as a clinical trial site

WHY CNS VERITAS

Strong Enrollment & Retention

Our established patient network and community outreach allow us to screen, enroll, and retain participants efficiently — reducing delays and dropout rates.

Experienced Principal Investigators

Our board-certified physicians bring deep expertise ensuring protocol adherence and scientific integrity.

Regulatory & Protocol Compliance

Every study is conducted in strict accordance with FDA regulations, ICH-GCP guidelines, and IRB-approved protocols — minimizing risk for sponsors.

High-Quality Data Collection

Our team is trained in accurate, consistent data capture using industry-standard EDC systems, ensuring clean, audit-ready data at every visit.

Operational Reliability

From site initiation to study close-out, our coordinators ensure timelines are met, queries are resolved promptly, and communication is seamless.

Focused & Efficient NYC Location

Our centralized New York City site provides a focused, well-managed environment with a consistent team across all sponsor studies.

OUR PROCESS

How our sponsor engagement works

Sponsor contacts our team with protocol details and therapeutic area.

1

Initial
Inquiry

We assess patient population, site capabilities, and protocol fit.

2

Feasaibility
Review
Site Qualification

IRB submission, contract execution, and site initiation visit.

3

Enrollment & Execution

Active recruitment, study visits, and real-time data entry.

4

Close-Out & Reporting

Data lock, query resolution, and regulatory document archiving.

5

1

Research you can trust — at every level

Compliance and standards

FDA 21 CFR Part 11 Compliant

All electronic records and signatures meet FDA requirements for data integrity and audit trails.

IRB-Approved Protocols

Every study is reviewed and approved by an Independent Review Board prior to initiation.

All staff are GCP-trained and studies are conducted in full accordance with international standards.

ICH Good Clinical Practice

Participant data is protected in strict compliance with HIPAA regulations and sponsor confidentiality agreements.

HIPAA & Data Privacy

GET IN TOUCH

Interested in partnering with CNS Veritas?

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