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Blog

Reporting to the IRB: Unanticipated Device Effects in Medical Device Studies

What do the regulations say about unanticipated device effects and IRB reporting? In this blog, Advarra addresses unique requirements for medical device studies.

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2 min. read
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Blog

How Centralized IBC Review Can Benefit Gene Therapy Research

Understand the risks and regulatory requirements for gene therapy research and how a biosafety review can benefit this type of research.

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4 min. read
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Blog

Local Versus Central IRBs: What’s the Difference?

Local IRBs and central IRBs are not really that different, although sIRB mandates have complicated things for local IRBs.

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3 min. read
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Blog

Virtual Symposium: Gene Therapy Research in the Age of COVID-19

The coronavirus pandemic has brought genetic research to the forefront. To address emerging issues, Advarra presents its first virtual symposium. Read more:

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2 min. read
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Blog

Keep in Touch: Tips for Working with a Single IRB for the First Time

Recent regulations and policies have many institutions establishing policies and processes for working with an external sIRB. Read more:

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7 min. read
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Blog

How Sites Can Prepare for COVID-19 Genetically Engineered Vaccine Studies

Is your site prepared to participate in COVID-19 vaccine research? Registering an IBC ahead of time gives you an advantage. Read more:

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4 min. read
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Blog

A Tale of Two Sites: The Power of Integrated Research Administration

Learn how institutions attract more studies from the the tale of two sites: one with an integrated research administration, and one without.

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5 min. read
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