Info Sheet
Electronic Study Design Services Overview
Advarra’s team of study design experts deliver high-quality calendars and forms in Advarra EDC utilizing best practices in data capture and form design.
Revised Common Rule Quick Reference
Most requirements for the revised Common Rule, the federal policy for the protection of human subjects in research, went into effect on January 21, 2019. This reference will help you: ...
CQA Compliance Oversight Programs
Advarra's customized evaluation and support services for clinical quality assurance (CQA) compliance help ensure your organization maintains appropriate compliance with applicable regulations and good clinical practice (GCP).
IBC-Ready™ Support
With IBC-Ready™, Advarra can help reduce confusion and administrative burden by coordinating with the sponsor, site personnel and local IBC(s) to complete local IBC submission forms.
IRB Services: Canadian Review
Advarra’s Canadian review service combines local, expert oversight with streamlined processes and the most extensive site reach in Canada.
IRB Services: Institutions, AMCs & Research Consortia
Advarra serves as your external support and compliance partner for everything from single investigational sites to multisite research consortia and therapeutic networks.
IRB Services Overview
Advarra's IRB services help empower better research programs and protect the rights and welfare of research participants.
Consulting Services Overview
Advarra's proactive, collaborative approach helps pharmaceutical, medical device, biopharmaceutical firms, as well as contract research organizations, academic institutions, health systems, and other research sites strengthen and grow their research enterprises.