Compliance Simplified, Success Amplified

We offer comprehensive regulatory management services designed to simplify every phase of the study lifecycle.

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Elevating Sites' Successes For Years With the Triallogix Difference

Our efforts have kept study teams focused and worry-free for years.

"Great service! They made managing our regulatory documents so much easier and kept everything on track. Highly recommend!"
Sarah V.
"Glad we went with them for our trials. We were getting overwhelmed by the time and hassle it took to get our budgets and contracts sorted and having them streamline and manage it for us was definitely worth it."
Allen M.

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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More Services

See how we can save you time, money, and energy

Reduce costly delays and offload the hassle of study start-up contracts and negotiations to our team

IRB Submissions
Regulatory Management
Training & Credential Tracking
Clinical Site Consulting Strategy
IRB Submissions & Oversight

From initial approvals to amendments and renewals, we ensure flawless execution.

Regulatory Document Management

Keep you files audit-ready and compliant with evolving standards.

Training & Credential Tracking

Maintain up-to-date staff qualifications and certifications to meet sponsor and regulatory requirements.

Clinical Site Consulting

Leverage our 25 years of experience operating one of the top performing clinical research sites in the United States

Our Commitment
to Excellence

At Triallogix, we are more than just a regulatory partner, we are a trusted ally dedicated to your success. Our track record of supporting over 500 studies demonstrates our ability to deliver results with precision and reliability.

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Frequently
Asked Questions

You have questions? We have answers. If you have other specific questions, please reach out to us at info@triallogix.io

What services does Triallogix provide?

Triallogix specializes in completing, submitting, and managing regulatory documents for clinical research sites. We ensure accuracy, compliance, and timely delivery of essential regulatory documentation.

What types of regulatory documents can Triallogix assist with?

We handle a wide range of documents, including but not limited to:
• 1572 Forms
• Financial Disclosure Forms
• Investigator CVs and Licenses
• Protocol Deviation Reports
• Safety Reports
• IRB Submission Packets
• Study Start-Up Documentation

How does Triallogix ensure compliance with regulations?

Our team of regulatory experts stays updated on the latest FDA, ICH-GCP, and IRB guidelines. We use quality assurance checks to ensure all documents meet regulatory standards.

Who can benefit from Triallogix services?

Clinical research sites, including independent sites, hospital-affiliated sites, and multi-site research organizations, can benefit from our streamlined approach to regulatory document management.

How does the Triallogix process work?

Step 1: Initial consultation to assess your needs.
Step 2: Collection of required information and documents.
Step 3: Preparation and review of regulatory documents.
Step 4: Submission to the appropriate regulatory body or sponsor.

Can Triallogix work with my existing regulatory systems or templates?

Yes, we can integrate with your current processes and use your preferred systems or templates to ensure a seamless workflow.

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Compliance Simplified,
Success Amplified

Avoid delays, increased costs, and potential compliance risks when you partner with Triallogix.

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