Our Trial Management Solutions

At Triallogix, we've helped research sites like yours successfully navigate regulatory compliance for over 500 studies --and counting.

Our Solutions

IRB Submissions & Oversight

By streamlining submissions, minimizing delays, and safeguarding against compliance risks, we can help you activate studies faster, maintain audit readiness, and build trust with sponsors and participants. Our expertise keeps your trials running smoothly, protects your site’s reputation, and positions you as a preferred partner for sponsors, all while saving you time and resources to focus on quality research.

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Our Solutions

Regulatory Document Management

Stay audit-ready at any moment --with us, your site’s regulatory documents will be meticulously organized, compliant, and ready for audits at any time. By ensuring every essential document is accurate, up-to-date, and easily accessible, we help you avoid compliance risks, maintain strong relationships with sponsors, and meet regulatory standards with confidence.

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The Triallogix Team

Our clinical research team combines scientific expertise with compassionate care. We are proud to uphold the highest industry standards, delivering reliable data and exceptional support for every clinical trial.

Kevin Oei, D.O.

Family Medicine/Urgent Care, Principal Investigator

Arjun Makam, D.O.

Cardiologist, Principal Investigator

Joanna Chan, M.D.

Dermatologist, Principal Investigator

The Clinical Staff

We partner with a wide range of physicians including a board certified Cardiologist and Dermatologist

The Research Team

We have a robust team that boasts over a decade of experience across all levels of clinical research

Sponsors Our Investigators Have Worked With

Why Work With Triallogix?

Triallogix is led by an actively practicing physician with direct oversight of study conduct, patient safety, and protocol adherence. Our clinical decision-making remains centralized, responsive, and aligned with sponsor and CRO expectations—ensuring efficient issue resolution and consistent execution.

Email us at info@triallogix.io
Patient-Centered Recruitment and Retention

We leverage an existing clinical patient population and structured screening processes to support efficient and compliant enrollment. Our approach emphasizes patient education, visit adherence, and long-term engagement, resulting in strong retention and reduced protocol deviations.

Built for Reliable Study Execution

Our site is purpose-built with standardized workflows, established SOPs, and trained research staff to support predictable performance across studies. We prioritize operational discipline, accurate feasibility assessments, and realistic enrollment commitments—reducing variability and execution risk for sponsors.

Regulatory and Audit Readiness from Day One

Triallogix maintains organized, continuously updated regulatory files and source documentation to support audit and inspection readiness at all times. We emphasize proactive compliance rather than reactive correction, supporting clean monitoring visits and smooth closeout processes.

Transparent Communication and Accountability

Triallogix values clear, timely communication with sponsors and CROs. We provide prompt feasibility responses, consistent updates, and early escalation of risks or challenges. Sponsors work directly with a site that takes ownership of outcomes—not one that defers responsibility.

Frequently
Asked Questions

Have questions about joining a clinical trial? Here are some of the most common things people want to know before they participate.

1. What type of clinical trials does Triallogix conduct?
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2. How does Triallogix ensure regulatory compliance and data integrity?
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3. What is Triallogix’s approach to study startup and timelines?
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4. How does Triallogix approach patient recruitment and retention?
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5. What differentiates Triallogix as a clinical trial site?
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