Clinical Research Administration

IRB Submission Management

This service handles the preparation and submission of all documentation required for Institutional Review Board (IRB) or ethics committee approval.

For Sites, it ensures timely, accurate submissions that reduce trial delays and avoid compliance issues.

For Sponsors and CROs, it accelerates study startup and enhances confidence in Site readiness and regulatory alignment.

Why Choose Vitalief

Sponsors, sites, and CROs choose Vitalief’s Clinical Research Administration services because we provide experienced professionals and proven processes that streamline trial execution and reduce administrative burden. Our support ensures regulatory compliance, timely documentation, and seamless coordination, enabling research teams to stay focused on quality, enrollment, and outcomes.

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