Universal Archives

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New Paper Makes the Case for AI-Specific Guidance in Research Oversight

AI is becoming a routine part of how research proposals are prepared and reviewed, from drafting applications to supporting administrative

Francine Lopez Senior Manager Client Services Advarra

Q&A with Senior Manager of Client Services Francine Lopez

For nearly a decade, Francine Lopez has helped clinical research move from idea to impact. From her early days at

Embedding AI And Critical IRB Operations Data To Drive Intelligent Study Design

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.

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Simplifying Oversight and Managing Regulatory Complexity in Multi-Site Clinical Trials

Traditional clinical trial designs often delay progress due to rigid protocols and frequent amendments. Adaptive and platform trial models introduce flexibility and shared infrastructure, reducing startup delays, cutting costs, and enabling sponsors to conduct faster, more efficient research.

Q&A with Advarra’s Client Experience Team Lead Jennifer DeZurik

Client Experience Team Lead Jennifer DeZurik brings both professional and deeply personal connections to Advarra and the world of clinical

How to Select a Clinical Trial Management System

Q&A with Advarra’s Associate Director of Client Services Anna Carnevale

Over the past 14 years, Anna Carnevale, associate director of client services at Advarra, has seen her team grow from

Building Customer Experiences That Lead to More Hope for Patients

Clinical research gives people hope. For some, it’s the chance to hold a new grandchild. For others, it’s walking a

A digital interface showing a person interacting with transparent virtual icons related to compliance, such as "Policies," "Regulations," "Audit," "Guideline," "Requirement," and "Law." The word "COMPLIANCE" is prominently displayed in the center, surrounded by hexagonal icons representing various regulatory and legal concepts.

The Impact of ICH E6(R3) on U.S. and Canadian IRBs

Now that FDA has published the ICH E6(R3) Good Clinical Practice (GCP) guidance, aligning early with these requirements can prepare organizations for the future. ICH E6(R3) encourages ethics review committees to more intelligently apply their resources by enhancing efficiency without compromising participant safety or data integrity particularly regarding continuing review, informed consent, decentralized logistics, and data governance. Sponsors partnering with Advarra can be confident that their studies remain regulation-ready on both sides of the border today and E6(R3)-ready for tomorrow.