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A Sponsor's Guide to Auditing IRBs: Detecting Deficiencies and Ensuring Best Practices

$357.00
June 2009
978-1-60004-054-2
48
Also Available:
Here is the one step-by-step management report that gives you the tools you need to determine if your IRBs are complying with federal regulations, including:
  • 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.

Order your copy of A Sponsor’s Guide to Auditing IRBs: Detecting Deficiencies and Ensuring Best Practices and discover how to avoid an IRB compliance disaster once and for all.

Buy Now!
See if your IRB is really complying with federal regulations — and fix problems before the FDA finds them. Order your copy of A Sponsor’s Guide to Auditing IRBs: Detecting Deficiencies and Ensuring Best Practices today. Priced at just $357, this must-have management report is available in PDF or print format.

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