Research Operations
Staying Connected and Compliant: Reimagining Clinical Trials with Longboat
Learn how Longboat is reimagining critical workflows across sites, sponsors, CROs, and patients.
Budgeting for IRB Review: A Guide for HRPP Leadership
Internal IRB reviews are NOT free, contrary to popular belief. In this blog we outline practical steps for assessing and establishing IRB review cost
Understanding the Impact of the New EU Artificial Intelligence Act on Clinical Research
Find out how the EU AI Act will likely impact clinical research software and systems, and what EU and non-EU entities should do to prepare for compliance.
Empowering Clinical Trials: The Pivotal Role of eSource
Our eBook outlines how eSource can make clinical research data more accessible, accurate, and reliable.
Preparing Your Action Plan for the FDA sIRB Mandate
Join our webinar for practical guidance from IRB thought leaders on what to include in your sIRB reliance preparations.
Overseeing and Operationalizing Patient Recruitment Across Study Stakeholders
This webinar for sponsors and CROs will tackle the most pressing challenge in clinical research: achieving enrollment targets on time.
Good Manufacturing Practices: When Do They Apply?
Ensure product quality and compliance in the drug development process. Learn how to optimize your manufacturing processes and maintain key regulatory standards with cGMP best practices from experts.
Conducting Research With CAR T Cells
This white paper is a guide for research professionals looking to conduct CAR T cell studies for the first time, as well as for those seeking to expand their existing portfolio.
4 KPIs Clinical Research Study Managers Can Master
This white paper examines four KPIs most impacting timelines and budgets and offers strategies for effective communication and risk mitigation.
Business Best Practices for Research Sites
Explore key process and technology focus areas for sites looking to improve their business strategies.
Developing a Data-driven Feasibility Process
Assessing feasibility in clinical research is vital for success, enabling organizations to make informed decisions and ensure seamless execution and reporting of studies.
The Regulatory Binder Checklist For Clinical Trial Sites
This checklist offers a comprehensive framework for managing all necessary essential regulatory documents efficiently.
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