FDA Proposes Revised IRB Regulations, Including Required sIRB for Multisite Trials
On September 28, 2022, the Food and Drug Administration (FDA) released two proposed rules, or Notices of Proposed Rule Making
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IRB and HRPP Advisory Services
STRATEGIC ENABLEMENT SERVICES HRPP/IRB Advisory Services Advarra’s Human Research Protection Program (HRPP)/Institutional Review Board (IRB) Advisory services include accreditation support,
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Welcome to Advarra’s Trust Center At Advarra, trust is the cornerstone of our relationships with clients, employees, and partners. Our
Advarra Innovation Summit | Cambridge, MA
Advarra Innovation Summit Cambridge, MA June 11, 2025 | 8:30 am – 5:00 pm ETLe Méridien Boston Cambridge Explore the
Ways to Streamline Informed Consent Process in Clinical Trial Startup
At a busy research site, a clinical trial is ready to launch — but it’s stuck in limbo over a
2025: Perspectives and Predictions From Advarra Thought Leaders
2024 has been a year of growth and evolution in clinical research. The coming year is expected to be no
Federal Grant Application Checklist
Navigate federal grant applications with Advarra’s expert checklist. Our streamlined process ensures compliance and participant protections for your research.
Institutional Review Board (IRB) Services
More than four decades of ethical review leadership Advarra is the largest central IRB, pairing scale with deep scientific, regulatory,
Oncology Clinical Research
SOLUTIONS FOR Oncology Clinical Research As a cancer research leader, you face unique challenges requiring specialized support and expertise. Whether