• Takeaway tactics you can use for FDA and HHS Office of Human Research Protection audits
• An overview of the regulatory requirements for clinical research
• Using an IRB accredited by the Association for the Accreditation of Human Research Protection Programs — what’s in it for you
• The shared responsibilities of patient protection — sponsor, IRB and researcher
• How to ensure that your IRB’s activities match written SOPs (including the documents and reports you should be asking for!)
• And so much more

With Congress threatening legislation that will fortify FDA and HHS oversight, you’ll need to act fast.

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