Coverage Analysis Contact Request
Simplify trial budgeting and billing with Advarra’s expert coverage analyses, designed to reduce errors and support efficient site operations.
Advarra Strategic Enablement Services
Focus on research while Advarra enhances compliance, accelerates timelines, and optimizes technology for clinical trial management.
Research Ready Training Contact Us
Prepare your teams for success with Advarra Research-Ready Training, designed to streamline trials and enhance compliance.
Study Activation Contact Request
Advarra’s study activation package delivers rapid results with budget support, coverage analysis, and tailored Clinical Conductor setups.
HRPP Assessment Contact Request
Advarra provides skilled interim staff for HRPPs and research compliance, from IRB managers to VP-level research administration professionals.
Consulting Contact Us
Enhance drug and device development with Advarra’s expert consulting, delivering solutions that prioritize quality and operational excellence.
DEI Contact Us
Improve diversity and inclusion in clinical research with Advarra’s global expertise in DE&I planning and recruitment strategy development.
BioPharma and MedTech Services Contact Us
Optimize study startup and execution with Advarra’s integrated solutions, including IRB/IBC reviews, consulting, and regulatory expertise.
Advarra Connect Contact Us
Save time with Advarra Connect, reducing effort by up to 15 minutes per document routed to your eTMF within a connected research ecosystem.
Advarra GPS
Advarra’s IRB support services help institutions streamline research while leveraging the world’s largest integrated IRB processes and technology.
2024 Site-Sponsor-CRO Collaboration Survey Report
The Site-Sponsor-CRO Collaboration Survey Report highlights challenges in collaboration, offering actionable insights from 200+ professionals to improve trials.
Materials Required for Submitting a Study to the IBC
Comprehensive IBC submissions require detailed materials, including investigator CVs, safety protocols, and site-specific SOPs for study agent handling.