Informed Consent Forms

Simplify study activation with expertly crafted informed consent forms that ensure compliance and clear communication for research participants.

Institutional Research Contact Request

Optimize workflows and boost efficiency with Advarra’s comprehensive services, from IRB reviews to specialized consulting and professional support.

Discover 1,500+ vetted sites worldwide ready for gene therapy and mRNA trials, offering streamlined startup and proven research capabilities.

Join the Gene Therapy Network to accelerate study activation, gain IBC support, and position your site as a preferred choice for sponsors.

Advarra’s biosafety experts streamline startup for gene therapy trials with comprehensive IBC reviews and proven rapid turnaround times.

Speak with an Advarra Calendars expert to explore solutions and insights for your current or future CTMS implementation needs.

Simplify trial budgeting and billing with Advarra’s expert coverage analyses, designed to reduce errors and support efficient site operations.

Focus on research while Advarra enhances compliance, accelerates timelines, and optimizes technology for clinical trial management.

Prepare your teams for success with Advarra Research-Ready Training, designed to streamline trials and enhance compliance.

Advarra’s study activation package delivers rapid results with budget support, coverage analysis, and tailored Clinical Conductor setups.

Advarra provides skilled interim staff for HRPPs and research compliance, from IRB managers to VP-level research administration professionals.

Enhance drug and device development with Advarra’s expert consulting, delivering solutions that prioritize quality and operational excellence.