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Recent Resources

 
Blog

Risk Assessment for use of Engineered Genetic Materials in Clinical Research

Learn why an institutional biosafety committee needs to complete a risk assessment for engineered genetic material in clinical research.

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4 min. read
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Webinar

Full Board vs Expedited vs Exempt: Why IRBs do That

Upcoming: April 20

A discussion on what IRBs must consider, what might tip the scales for a study that could go either way, and what “expedited review” means.

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Blog

How Single IRB Review Mandates Help Research Sponsors

The proposed single IRB mandates will impact FDA-regulated research, potentially altering existing practices at organizations.

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4 min. read
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