
Seeking faster startup for cell and gene therapy studies? Sponsors can streamline IRB and IBC reviews by coordinating the committees’ activities via a vendor offering both resources in-house.
Seeking faster startup for cell and gene therapy studies? Sponsors can streamline IRB and IBC reviews by coordinating the committees’ activities via a vendor offering both resources in-house.
Curious about mRNA technology and the regulatory requirements for its use in clinical trials? Advarra’s gene therapy research experts respond to commonly asked questions.
How can you tell if your study requires IBC oversight? Start with these common terms found in research protocols requiring IBC review.
Explore how an integrated approach to the clinical research industry’s technology landscape can remove friction, improve access and diversity, save time, and better serve patients.
Download this report to learn how the COVID-19 pandemic impacted the future of the clinical research workforce.
Download this report to learn how the COVID-19 pandemic impacted the future of the clinical research workforce.
Download this report to learn how the COVID-19 pandemic impacted the future of the clinical research workforce.
*** Wednesday, May 26, 2021 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST *** It has never been more important for sponsors, monitors, and sites to learn how best to conduct monitoring visits remotely and securely. Learn about implementing remote monitoring, including analyzing implementation challenges, understanding the FDA’s guidance on delayed monitoring, and more. ***On demand available after final airing until May 26, 2022***
Find out how traditional trial modalities have evolved to participant-centric virtual platforms and how to best engage your IRB in this Advarra-Science 37 collaboration.
Traditional paper-based processes are rapidly being replaced with electronic tools for more efficient and accurate clinical trials conduct. This whitepaper will help research sites prepare for the electronic future.
Traditional paper-based processes are rapidly being replaced with electronic tools for more efficient and accurate clinical trials conduct. This whitepaper will help research sites prepare for the electronic future.
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