IIT- Protocol Amendments
Course DescriptionNasrin Babadi, PhD takes you through LCCC’s processes for amending protocols and submitting them to FDA talking about key tips on how to best edit your protocol and applicable FDA regulations for submitting your protocol.
Category
Format
  • Self-Paced, Online Courses
Credits
  • 1.00 Participation
IND Safety Reporting- LCCC IITs
Course DescriptionIn this talk, Kaitlin Morrison, PhD covers how to fill out a MedWatch report form and how/when/why to notify FDA of an SAE.
Category
Format
  • Self-Paced, Online Courses
Credits
  • 1.00 Participation
LCCC’s Single Subject Exception Policy
Course DescriptionIn this talk by Kaitlin Morrison, PhD and Carrie Lee, MD, MPH, Kaitlin takes your through LCCC’s policy on single subject exceptions, why we do not allow eligibility single subject exceptions on IITs and what the process is to ensure
Category
Format
  • Self-Paced, Online Courses
Credits
  • 1.00 Participation
Project Management of CPO Trial Activation 101
Course DescriptionThis lecture takes you through business principles as defined by “Project Management: A Systems Approach to Planning, Scheduling and Controlling” by Harold Kernzer. Kaitlin Morrison, PhD will cover what is traditional vs.
Category
Format
  • Self-Paced, Online Courses
Credits
  • 1.00 Participation
Protocol Amendments vs. Administrative Letters
Course DescriptionIn this talk, Kaitlin Morrison, PhD discussing what an administrative letter is and when an administrative letter can be used to clarify a clinical protocol versus when a full amendment is required. 
Category
Format
  • Self-Paced, Online Courses
Credits
  • 1.00 Participation
IND Boot Camp
Course DescriptionIn this talk, targeted at the CPO regulatory team, Kaitlin Morrison, PhD talks through how INDs are maintained at LCCC and the responsibilities of study team members.
Category
Format
  • Self-Paced, Online Courses
Credits
  • 1.00 Participation
Two Successful Clinical Trialists Reflect on How They Got Their Start
Course DescriptionClaire Dees, MD, talks with Jared Weiss, MD and Carey Anders, MD, about their early experiences in running a clinical trial, including investigator-initiated clinical trials.
Category
Format
  • Self-Paced, Online Courses
Credits
  • 1.00 Participation
Understanding when Assays become Investigational Assays
Course DescriptionIn this talk Mike Matamoros, MS, CIP and Cassie Myers, CIP take you through IRB regulations about investigational assays, using COVID-19 assays as examples. 
Category
  • Investigator Initiated Trials
Format
  • Self-Paced, Online Courses
Credits
  • 1.00 Participation
What is a “Critical Path” and How Can it Help Me?
Course DescriptionKaitlin Morrison, PhD takes you through the business principles of critical paths, PERT charts and Gantt charts and how they can be used to streamline clinical trial activation.
Category
  • Investigator Initiated Trials
Format
  • Self-Paced, Online Courses
Credits
  • 1.00 Participation
Working with Investigational Assay Results
Course DescriptionKaitlin Morrison, PhD takes you through when a correlative assay is considered an FDA regulated device and what types of devices require different levels of IRB and FDA approval.
Category
Format
  • Self-Paced, Online Courses
Credits
  • 1.00 Participation

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