Join Advarra

Learn more about our company team, careers, and values. Join Advarra’s Talented team to take on engaging work in a dynamic environment.

See Jobs

How to Be Research Ready: Today and Beyond

A study opportunity is presented to your organization. How quickly and confidently could you take on the study? This is the concept of research readiness. Research readiness, when put into practice, ensures that your organization can accept, activate, and adapt to new studies and opportunities no matter the regulatory circumstances, be it decentralized structure, protocol complexity, or even a global pandemic.

To be research ready, your organization must have:

No other system supports research readiness like an eRegulatory Management System. An eRegulatory management system can centralize your training, documentation, processes, and communication needed to efficiently and compliantly activate a trial. In collaboration with leading academic research institutions and cancer centers, Advarra eRegulatory Management System (eReg) has evolved to comprehensively support and ensure research readiness.

This past year has displayed firsthand that the definition and expectations of research readiness can change dramatically. When COVID-19 hit, many organizations found themselves without the necessary processes and infrastructure to conduct research or accept new studies, hurting their research goals and delaying activation timelines. That’s why we’re ensuring Advarra eReg is not only research ready today, but also built for the future.

Immediate Document Access from Anywhere

Access, route, store, and centralize staff credentials, standard operating procedures (SOPs), organization documents, and past performance documents to streamline regulatory workflows from any site location.

Integrated Processes

Leverage integrations with key regulatory systems within Advarra eReg including eIRB and local IRBs, OnCore Clinical Trial Management System (CTMS), and email correspondence to increase compliance and efficiency.

Community-Driven Workflows

Benefit from innovations by regulatory teams like yours. Utilize standardized workflows developed with community in mind including regulatory templates, digest notifications, and controlled and secured monitor access.

A Future-Proof eRegulatory System

Maintaining a research ready state requires a successful foundation for an ever-evolving industry. Advarra eRegulatory Management System is preparing for the future of clinical trials by expanding our solution to serve across the entire stakeholder spectrum, from sponsors to sites. We’re working closely with our customer community to maintain site-centricity as we expand integrations both inside and outside the Advarra ecosystem including connections with eConsent tools, OnCore CTMS documents, sponsor platforms, and more.

To explore recently released features in Advarra eReg and discuss how we’re building an eRegulatory management system that supports research readiness in the future, attend our Advarra eReg Open Demo.

Back to Resources