David Forster, JD, MA, CIP | Chief Compliance Officer
Mr. Forster joined Western IRB (WIRB) in 1996 and is currently the Chief Compliance Officer for the WIRB-Copernicus Group (WCG). A strong advocate for human subject protections, Mr. Forster co-chairs the Secretary’s Advisory Committee on Human Research Protections (SACHRP) Sub-Committee on Harmonization. He previously served a four-year term as a member of SACHRP, and was previously a member of the SACHRP Sub-Committee on Inclusion of Individuals with Impaired Decision-Making in Research. Mr. Forster also served on the Certified IRB Professional (CIP) Council.
Mr. Forster has a law degree and a Masters in Medical Ethics from the University of Washington.
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How do I handle a deviation in the use of blood specimens collected outside the timeframe?
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How should a site document a missing signature on a HIPAA authorization form?
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How should we handle financial conflicts of interest in FDA-regulated clinical trials?
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Returning Study Results to Research Participants
Studies show clinical trial participants want to know what was learned from their involvement. Many sponsors are implementing plans to deliver plain language summaries to trial participants.
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Addressing the Challenges of Human Tissues and Cell Products Regulation
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