Advarra, Author at Advarra | Page 2 of 5

Skip to content

Search...

About
Careers
Login

IRB
- IRB Services
- IRB Resources
Solutions
Platform
- Advarra’s Data & AI Engine, Braid™
Resources
- Learn
- Community
Contact

Search...

Advarra

Latest Posts by Advarra

Sponsor’s Guide to IRB Approval (Part V): How to Speed Up IRB Approvals

Institutional review board (IRB) approval is a critical milestone in clinical research, but it can...

Sponsor’s Guide to IRB Approval (Part IV): Preparing IRB Documents That Prevent Delays

A strong protocol and well-drafted consent form are essential, but they are not enough on...

Q&A with Advarra’s Associate Director of Client Success Evan Sander

Evan Sander knows firsthand that clinical research is never just about processes or paperwork—it’s about...

Advarra’s Study Design Solution Named “Best Clinical Study Design Solution” in 2026 MedTech Breakthrough Awards Program

Landmark 10th annual awards program, which received over 5,000 entries, recognizes the most innovative digital health and medical technology solutions worldwide COLUMBIA, Md., – May 7, 2026...

Sponsor’s Guide to IRB Approval (Part III): Building an IRB-Ready Informed Consent

For sponsors, informed consent is one of the most visible signals of study quality during...

A More Connected Approach to Clinical Trials: Reducing Friction from Study Design Through Conduct

Clinical trials are complex. That’s expected, given accelerated advancements in science and technology. But when...

Sponsor’s Guide to IRB Approval (Part II): How to Draft a Clinical Trial Protocol That Stands Up to IRB Scrutiny

A strong clinical trial protocol does more than describe how a study will run. It...

Photo of real female scientists researching in laboratory.

Emerging Use of Bacteriophages, Natural Predators of Bacteria, to Combat Antibiotic Resistance in the Clinic and Beyond: A Review of the Field and Biosafety Assessment

Explore the latest research on bacteriophage therapy, including advances in clinical development, biosafety, and regulation.

New Framework Proposes Risk-Based Governance for AI in Clinical Development

First deliverable from the Council for Responsible Use of AI in Clinical Trials, a cross-industry...

Sponsor’s Guide to IRB Approval: What Every Sponsor Needs to Know Before Submitting a Study

Introducing the ‘Sponsor’s Guide to IRB Approval’ Institutional review board (IRB) approval protects the rights, safety, and...

Q&A with Advarra’s Director of Training in IRB Services Lori Young

Lori Young has spent her career at the intersection of research, ethics, and education—and her...

Advarra to Showcase Technology Innovations for Research Sites at Onsemble 2026

Columbia, MD – April 2, 2026 – Advarra, the industry leader in integrated solutions for...

Unlock Novel Operational Intelligence and Automation in Clinical Trials

IRB

IRB Services 
IRB Resources

Solutions for Sponsors & CROs

Study Design
Site Identification & Feasibility
Study Startup
Site Collaboration & Training
Enrollment Planning & Tracking

Solutions for Sites & Institutions

CTMS
OnCore
Clinical Conductor
eReg
eSource
Strategic Enablement Services

Contact us

Resources

Blog
Newsroom
Acronyms Library
Advarra Voice

Community

Onsemble Conference
Innovation Summits

About

About Advarra
Leadership Team

Advarra Trust Center
Privacy Policy
Cookie Policy
Terms of Use

© 2026 Advarra

Login

Search for:

IRB
- IRB Services
- IRB Resources
Solutions
Platform
- Advarra’s Data & AI Engine, Braid™
Resources
- Learn
- Community
About
Careers at Advarra
Contact

IRB
- IRB Services
- IRB Resources
Solutions
Platform
- Advarra’s Data & AI Engine, Braid™
Resources
- Learn
- Community
About
Careers at Advarra
Contact

Scroll to Top