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YCCI Training Sessions for New Staff: "Introduction to Research Principles"

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This course will provide a review of ICH E6 Guidelines plus FDA and OHRP Regulations, discuss fundamentals of Informed Consent and help attendees to understand post-initial approval regulatory requirements, including IRB Reporting. This small group course are intended for those involved in non-cancer research and is ideal for new coordinators or those who are new to Yale.
Hosted by Pat Seymour, Associate Director for Regulatory Affairs, YCCI.
Please note: This course focuses on the application of GCP in your role. The course is not designed to fulfill GCP Training requirements/recommendations by the NIH or Industry Sponsors.


  • Patricia Seymour




Free: free


Lectures and Seminars, Training


Snacks: Refreshments.
Feb 201724Friday
9:00 AM12:00 PM
Basement Conference Room2 Church St SNew Haven, CT