Info Sheet

Designed to be a starting point for grant conversations at your organization, this identifies elements to include in applications and budgets.

Secure Document Exchange offers a site-centric approach to managing and exchanging regulatory documents among sites, sponsors, and CROs.

Advarra's research billing services can ensure proper research billing compliance, administration, and operations.

Download the info sheet to learn about IRB review of cosmetics research, including applicable regulations and the IRB’s role.

Advarra's HRPP services can keep your research moving forward, improve compliance and collaboration, and streamline IRB review processes.

Advarra has the unique product expertise and ability to fulfill multiple clinical research technology roles

Advarra provides highly qualified research professionals to fill critical interim roles and responsibilities in clinical research operations

This info sheet describes Advarra’s Gene Therapy Ready site network and the benefits of joining the network

View this info sheet to learn about Advarra’s IRB expert oversight and guidance to support your next federal grant proposal.

Download tips and considerations for sponsors and IRBs for next research project involving exception from informed consent (EFIC)

Learn how Advarra’s Clinical Conductor Study Build services expedites study activation, saves time, and increases protocol compliance.

Advarra provides interim staffing for research administration, HRPPs, institutional review boards, and other research compliance programs.