Clinical QA Consulting For Medical Device Research
The medical device experts at Advarra can help you navigate the regulatory environment to ensure compliant, high-quality clinical study conduct.
GxP Auditing, Compliance, & Specialized Consulting
Advarra's experts can work directly with your team to provide consulting and evaluation services related to Good Practices, quality assurance, regulatory compliance, and human research protection for research.
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 to aid you in the conduct of efficient, responsible research.
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: Study Startup Support
Advarra provides flexible solutions that help accelerate the initial IRB review process and make it more efficient.
IRB Services: Central Oncology Review
Advarra’s Central Oncology Review service provides robust human subject protections review that cancer research institutions expect.
Technology Overview
Advarra's proven technology solutions complement research programs and operational strategies to help clients reach study milestones faster.