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.
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.
Host
Admission
Free: free
Tags
Lectures and Seminars, Training
Food
Snacks: Refreshments.