Q&A with Advarra’s new Senior Vice President, FDA Regulatory Advisor, Jan Hewett
Clinical research drives medical progress. Advarra ensures participant safety and ethical standards through expert IRB oversight for life-changing therapies.
Clinical research drives medical progress. Advarra ensures participant safety and ethical standards through expert IRB oversight for life-changing therapies.
Clinical research drives medical progress. Advarra ensures participant safety and ethical standards through expert IRB oversight for life-changing therapies.
Advarra’s commitment to ethical clinical research for over 35 years drives medical breakthroughs, ensuring participant safety and enhancing treatment options.
Launched in January 2025, the Association of Multisite Research Corporations (AMRC) was set up by its founding members to advance
Our webinar discusses key near-term trends and regulations and investigate persistent challenges frequently throwing even the most efficient teams off track. Advarra and industry representatives will dive deeper into achieving critical milestones across study startup, conduct, and close out that every project manager should optimize.
Timelines for study start-up affect everything from budgets and drug pricing to a site’s ability to secure trials. This webinar
Fostering knowledge exchange across the cancer research community Timely discussions. Expert perspectives. Illuminating the path to progress. Fostering knowledge exchange
This white paper examines four KPIs most impacting timelines and budgets and offers strategies for effective communication and risk mitigation.
This white paper examines four KPIs most impacting timelines and budgets and offers strategies for effective communication and risk mitigation.
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Site-Sponsor Consortium Building shared industry standards through collaboration The Site-Sponsor Consortium is an invitation-only forum that brings together influential leaders