Info Sheet

Negotiation can be one of the most time-consuming components in clinical trial start up activities. Rely on Advarra’s expertise, resources, and quick turnaround time to help ensure you achieve your funding goals.

Ensure your site stays in compliance with Medicare billing compliance regulations with industry standard methods combined with national and regional coverage determinations and proprietary solutions.

What is an IBC? How long does an IBC review take? Read our IBC 101 handout to get answers to some of your most frequently asked questions.

Research organizations manage many complex trials, often with limited resources. It can be difficult to gain insight into activities across all protocols. The clinical research management module in the OnCore Enterprise Research System supports centralized management of all protocols and subjects in one place.

Advarra’s Central Oncology Review service provides robust human subject protections review that cancer research institutions expect.

The Advarra eRegulatory Management System (eReg) was developed through close collaboration with leading research institutions to help improve your regulatory process and enhance regulatory compliance across your organization.

Adapt workflows as sponsors, CROs, sites, and institutions continue to meet the unprecedented circumstances of the COVID-19 pandemic. Advarra is here to assist with guidance and resources to help move ...

As a clinical research organization, choosing the right electronic data capture (EDC) system can be a challenge.

Address Medicare’s unique coverage decisions and improve your research program when Advarra evaluates your drug, device, or biological clinical trial and develops a coverage analysis to help you build your budget template.

Advarra knows that one size does not fit all. Each research program is different, with unique needs and distinct personalities. We take time to carefully understand your process and then ...