Understanding Regulatory Documents For Clinical Research Sites Webinar
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- The University Of
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- This 1-hour session will focus on Institutional Review Board (IRB)
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Detailed Analysis of Regulatory Documents For Clinical Research Sites Webinar
Essential Presenters: Natalie Hurst and Sandra Brindis, FHI 360. Thank you to my Sponsors: Versatrial: http://www.versatrial.io CRIO: http://www.
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