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Pre-Reg Required
New for 2020
New for 2020
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CSP Icon
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Livestreaming Session Icon
On-Demand Session
On-Demand Session
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CIP Accredited
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Additional Fee
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Pre-Reg Required
New for 2020
New for 2020
Part I/II
Part I/II
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CSP Icon
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Livestreaming Session Icon
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Prerecorded Session Icon
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CIP Accredited
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Browse by Track

Browse by Track

  • Wednesday, Nov 17th
    11:45 AM – 12:45 PM ET
    A02 - Knock, Knock, FDA Is Here: What You Need to Know for Bioresearch Monitoring (BIMO) Inspections of IRBs, Clinical Investigators, and Sponsor Investigators
    Location: Livestreamed
    FDA Regulated Research Track
  • Wednesday, Nov 17th
    1:45 PM – 2:45 PM ET
    B04 - When Is an Investigational Device Exemption (IDE) Needed for Medical Device Clinical Investigations?
    Location: Livestreamed
    FDA Regulated Research Track
  • Thursday, Nov 18th
    1:30 PM – 2:30 PM ET
    D01 - A Dialogue With FDA
    Location: Livestreamed
    A Dialogue With the Feds TrackFDA Regulated Research Track
    Sponsored By 
  • Friday, Nov 19th
    1:30 PM – 2:30 PM ET
    F03 - The IRB’s Critical Role in Understanding Sponsor and Investigator Responsibilities for Investigational New Drug Application (IND) Safety Reporting in Order to Assure the Protection of Human Subjects
    Location: Livestreamed
    FDA Regulated Research Track