Media Summary: This course provides the basic concepts of what clinical research is, how it is carried out and by whom, and its underlying ethical ... This webinar reviews the main regulations and policies that govern clinical trial registration and results reporting. It also describes ... This webinar introduces the role of sponsor-investigator in a clinical trial and discusses regulatory and study management ...

Citi Program - Detailed Analysis & Overview

This course provides the basic concepts of what clinical research is, how it is carried out and by whom, and its underlying ethical ... This webinar reviews the main regulations and policies that govern clinical trial registration and results reporting. It also describes ... This webinar introduces the role of sponsor-investigator in a clinical trial and discusses regulatory and study management ... This video shows you how to register for the A foundational course for individuals considering a career as a clinical research associate (CRA). The course provides broad ... The course describes the ICH's Guideline for Good Clinical Practice E6(R3). E6(R3) includes several updates from E6(R2).

This webinar explores the distinct ethical paradigm governing PCTs compared to conventional clinical research, rooted in ... Well-planned and executed study start-ups are an important part of efficient and effective clinical trials. This webinar describes the ... The webinar highlights the importance of clinical data managers during the conduct of a clinical trial and outlines the process of ... This webinar explores how the concept of race is used in clinical research, and the ethical and regulatory questions we need to ... This webinar discusses medical marijuana and related cannabis products, unique challenges and issues for research, and the ...

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CITI Program Course Preview - Clinical Research: An Introduction
CITI Program Webinar Demo - Building a ClinicalTrials.gov Compliance Program
CITI Training for Biomedical Research
CITI Program Webinar Demo - A Beginner’s Guide to Being a Sponsor-Investigator
How to register for CITI training
CITI Program Course Preview - Clinical Research Associate (CRA)
CITI Program - Informed Consent Case Videos
CITI Program Course Preview - ICH E6(R3): An Introduction
CITI Program Webinar Demo - Pragmatic Clinical Trials: What Hospitals and IRBs Need to Know
CITI Program Webinar Demo - Study Start-Up: Challenges and Strategies
CITI Program Webinar Demo - The Role of Data Managers in Clinical Trials
CITI Program Webinar Demo - Race in Clinical Research: Ethics and IRB Decision Making
View Detailed Profile
CITI Program Course Preview - Clinical Research: An Introduction

CITI Program Course Preview - Clinical Research: An Introduction

This course provides the basic concepts of what clinical research is, how it is carried out and by whom, and its underlying ethical ...

CITI Program Webinar Demo - Building a ClinicalTrials.gov Compliance Program

CITI Program Webinar Demo - Building a ClinicalTrials.gov Compliance Program

This webinar reviews the main regulations and policies that govern clinical trial registration and results reporting. It also describes ...

CITI Training for Biomedical Research

CITI Training for Biomedical Research

This video covers the

CITI Program Webinar Demo - A Beginner’s Guide to Being a Sponsor-Investigator

CITI Program Webinar Demo - A Beginner’s Guide to Being a Sponsor-Investigator

This webinar introduces the role of sponsor-investigator in a clinical trial and discusses regulatory and study management ...

How to register for CITI training

How to register for CITI training

This video shows you how to register for the

CITI Program Course Preview - Clinical Research Associate (CRA)

CITI Program Course Preview - Clinical Research Associate (CRA)

A foundational course for individuals considering a career as a clinical research associate (CRA). The course provides broad ...

CITI Program - Informed Consent Case Videos

CITI Program - Informed Consent Case Videos

CITI Program

CITI Program Course Preview - ICH E6(R3): An Introduction

CITI Program Course Preview - ICH E6(R3): An Introduction

The course describes the ICH's Guideline for Good Clinical Practice E6(R3). E6(R3) includes several updates from E6(R2).

CITI Program Webinar Demo - Pragmatic Clinical Trials: What Hospitals and IRBs Need to Know

CITI Program Webinar Demo - Pragmatic Clinical Trials: What Hospitals and IRBs Need to Know

This webinar explores the distinct ethical paradigm governing PCTs compared to conventional clinical research, rooted in ...

CITI Program Webinar Demo - Study Start-Up: Challenges and Strategies

CITI Program Webinar Demo - Study Start-Up: Challenges and Strategies

Well-planned and executed study start-ups are an important part of efficient and effective clinical trials. This webinar describes the ...

CITI Program Webinar Demo - The Role of Data Managers in Clinical Trials

CITI Program Webinar Demo - The Role of Data Managers in Clinical Trials

The webinar highlights the importance of clinical data managers during the conduct of a clinical trial and outlines the process of ...

CITI Program Webinar Demo - Race in Clinical Research: Ethics and IRB Decision Making

CITI Program Webinar Demo - Race in Clinical Research: Ethics and IRB Decision Making

This webinar explores how the concept of race is used in clinical research, and the ethical and regulatory questions we need to ...

CITI Program Webinar Demo - Medical Marijuana: A Budding Field of Research

CITI Program Webinar Demo - Medical Marijuana: A Budding Field of Research

This webinar discusses medical marijuana and related cannabis products, unique challenges and issues for research, and the ...