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Patient Workflow
Biopoint enhances patient safety and access to care. View our patient workflow technology solutions for sites.
mRNA Cancer Vaccines and Therapies: An Overview
Learn about mRNA’s potential impact on cancer research, the technology’s unique challenges, and strategies for researchers developing mRNA-based cancer studies.
DMC vs EAC: What’s the Difference?
This blog outlines the requirements for each committee, what it does, and the critical roles each plays in keeping research participants safe.
Compliance Date for Common Rule Revisions Delayed an Additional 6 Months
US federal departments and agencies have published a final rule delaying the revised Common Rule general compliance date to January 21, 2019.
Making a Case for Interim HRPP Staffing
Don't wait to fill an HRPP position until it's too late. Understand the risks of an understaffed HRPP and how interim staffing support can help. Read more:
Q&A Part 2 – Gene Therapy Research in the Age of COVID-19
Expert panelists from Advarra’s gene therapy virtual symposium address some of the most popular questions submitted by the audience. Read part 2:
International Research and Research Ethics Review
Clinical research continues to grow throughout the world, with researchers looking outside the US for new and diverse subject populations to help develop and improve investigational therapies. Lauri Carlile, VP of Operations at Advarra, discusses the basics of ex-US research ethics review for US-based researchers.
Gene Therapy Ready Site Network
Registered with the NIH as the IBC of record for over 1,000 research sites that are vetted and prepared to conduct your next clinical trial.
The Clinical Research Training Program Checklist: What to Look For
Most training programs are outdated, unengaging, & redundant. Learn how to make a program achieving both regulatory requirements & your goals
Improve Data Quality With 5 Fundamentals of Clinical Data Management
Learn more about how you can improve your clinical research data quality with these five fundamentals of clinical data management.
7 Staff Augmentation Resources to Help Your Site Restart Research
Advarra offers a number of services to help you restart your short- or long-term research activities, such as Staff Augmentation.
FDA Communications Through the Drug Development Lifecycle
Understand how to effectively communicate and build a relationship with the FDA throughout the drug development lifecycle.
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