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CITI Program offers research, ethics, and compliance training courses, as well as CME/CEU certified courses for a wide range of industries. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE We use cookies and other tracking technologies to recognize your repeat visits and preferences, as well as to analyze traffic and measure the effectiveness of communications. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE GOOD CLINICAL PRACTICE (GCP) Good Clinical Practice (GCP) includes basic courses tailored to the different types of clinical research. These courses also include corresponding refresher courses for retraining and advanced learning. CITI Program GCP training is used by over 1,500 institutions - (including many leading hospitals, academic medical centers,universities, and
HUMAN SUBJECTS RESEARCH (HSR) Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE).They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards(IRBs).
SHIPPING AND TRANSPORT OF REGULATED BIOLOGICAL MATERIALS Shipping and Transport of Regulated Biological Materials is designed as initial training and periodic retraining for employees who package or ship diagnostic and clinical human or animal specimens, human or animal pathogens, and other regulated biohazards. RESEARCH, ETHICS, AND COMPLIANCE TRAINING The Trusted Standard in Research, Ethics, and Compliance Training The Collaborative Institutional Training Initiative (CITI Program) is dedicated to serving the training needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - Collaborative Institutional Training Initiative. English Español Português 한국어 中文 Русский Français Tiếng Việt. New to the CITI Program? Read the getting started guide or CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. Use this option if you are paying for your courses. This option is for persons not affiliated with a CITI Program subscriber organization, or who require content that their organization does not provide. Fees apply. Credit card payment with American Express, Discover, MasterCard or Visa is required.Checks are
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CITI Program offers research, ethics, and compliance training courses, as well as CME/CEU certified courses for a wide range of industries. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE We use cookies and other tracking technologies to recognize your repeat visits and preferences, as well as to analyze traffic and measure the effectiveness of communications. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE GOOD CLINICAL PRACTICE (GCP) Good Clinical Practice (GCP) includes basic courses tailored to the different types of clinical research. These courses also include corresponding refresher courses for retraining and advanced learning. CITI Program GCP training is used by over 1,500 institutions - (including many leading hospitals, academic medical centers,universities, and
HUMAN SUBJECTS RESEARCH (HSR) Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE).They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards(IRBs).
SHIPPING AND TRANSPORT OF REGULATED BIOLOGICAL MATERIALS Shipping and Transport of Regulated Biological Materials is designed as initial training and periodic retraining for employees who package or ship diagnostic and clinical human or animal specimens, human or animal pathogens, and other regulated biohazards.EXPLORE OUR COURSES
CITI Program offers research, ethics, and compliance training courses, as well as CME/CEU certified courses for a wide range of industries. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE We use cookies and other tracking technologies to recognize your repeat visits and preferences, as well as to analyze traffic and measure the effectiveness of communications. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Decentralized Clinical Trials (DCTs) and Your Workforce $49.00 Have an account? LOGIN TO PURCHASE. Don't have an account? REGISTER TOPURCHASE
WHAT YOU NEED TO KNOW ABOUT COVID-19 VACCINE (FREE WEBINAR The webinar is intended to educate persons who may be involved with the administration of these vaccines by addressing many of the major concerns and questions that have been raised about these vaccines. This course is available at no cost to independent learners by affiliating with “COVID-19 Free Training (IL)” during the registration process. HUMAN SUBJECTS RESEARCH (HSR) Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE).They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards(IRBs).
CLINICAL RESEARCH COORDINATOR (CRC) CRC courses provide foundational and advanced role-based training for clinical research professionals. The courses cover information that expands beyond but is directly connected to the Human Subjects Research (HSR) and Good Clinical Practice (GCP) courses. The Foundations course delivers basic CRC training that organizations may use for onboarding new CRCs. RESPONSIBLE CONDUCT OF RESEARCH (RCR) The Communicating Research Findings course is beneficial to all researchers as it focuses on effective practices, guidelines, and strategies for communicating and presenting research findings.Organizations may add the modules in this course to the RCR Basic course or a Human Subjects Research (HSR) course or offer it to their learners on a standalone basis. IRB – SOCIAL-BEHAVIORAL-EDUCATIONAL FOCUS About this Course. This course is for IRB members who review social-behavioral-educational research. It provides an overview of IRB responsibilities, tools, and expectations. It also offers historic and current information on regulatory and ethical issues important to the conduct of social-behavioral-educational research involving humansubjects.
REGISTER NOW: PRIVACY AND ETHICAL CONSIDERATIONS FOR This webinar provides an overview of what makes CAVs different from the cars of yesteryear, an overview of privacy and ethics, and an overview of the privacy and ethical challenges raised by CAVs. RESEARCH, ETHICS, AND COMPLIANCE TRAINING The Trusted Standard in Research, Ethics, and Compliance Training The Collaborative Institutional Training Initiative (CITI Program) is dedicated to serving the training needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - Collaborative Institutional Training Initiative. English Español Português 한국어 中文 Русский Français Tiếng Việt. New to the CITI Program? Read the getting started guide or CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. Use this option if you are paying for your courses. This option is for persons not affiliated with a CITI Program subscriber organization, or who require content that their organization does not provide. Fees apply. Credit card payment with American Express, Discover, MasterCard or Visa is required.Checks are
EXPLORE OUR COURSES
CITI Program offers research, ethics, and compliance training courses, as well as CME/CEU certified courses for a wide range of industries. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE We use cookies and other tracking technologies to recognize your repeat visits and preferences, as well as to analyze traffic and measure the effectiveness of communications. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE GOOD CLINICAL PRACTICE (GCP) Good Clinical Practice (GCP) includes basic courses tailored to the different types of clinical research. These courses also include corresponding refresher courses for retraining and advanced learning. CITI Program GCP training is used by over 1,500 institutions - (including many leading hospitals, academic medical centers,universities, and
HUMAN SUBJECTS RESEARCH (HSR) Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE).They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards(IRBs).
SHIPPING AND TRANSPORT OF REGULATED BIOLOGICAL MATERIALS Shipping and Transport of Regulated Biological Materials is designed as initial training and periodic retraining for employees who package or ship diagnostic and clinical human or animal specimens, human or animal pathogens, and other regulated biohazards. RESEARCH, ETHICS, AND COMPLIANCE TRAINING The Trusted Standard in Research, Ethics, and Compliance Training The Collaborative Institutional Training Initiative (CITI Program) is dedicated to serving the training needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - Collaborative Institutional Training Initiative. English Español Português 한국어 中文 Русский Français Tiếng Việt. New to the CITI Program? Read the getting started guide or CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. Use this option if you are paying for your courses. This option is for persons not affiliated with a CITI Program subscriber organization, or who require content that their organization does not provide. Fees apply. Credit card payment with American Express, Discover, MasterCard or Visa is required.Checks are
EXPLORE OUR COURSES
CITI Program offers research, ethics, and compliance training courses, as well as CME/CEU certified courses for a wide range of industries. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE We use cookies and other tracking technologies to recognize your repeat visits and preferences, as well as to analyze traffic and measure the effectiveness of communications. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE GOOD CLINICAL PRACTICE (GCP) Good Clinical Practice (GCP) includes basic courses tailored to the different types of clinical research. These courses also include corresponding refresher courses for retraining and advanced learning. CITI Program GCP training is used by over 1,500 institutions - (including many leading hospitals, academic medical centers,universities, and
HUMAN SUBJECTS RESEARCH (HSR) Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE).They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards(IRBs).
SHIPPING AND TRANSPORT OF REGULATED BIOLOGICAL MATERIALS Shipping and Transport of Regulated Biological Materials is designed as initial training and periodic retraining for employees who package or ship diagnostic and clinical human or animal specimens, human or animal pathogens, and other regulated biohazards.EXPLORE OUR COURSES
CITI Program offers research, ethics, and compliance training courses, as well as CME/CEU certified courses for a wide range of industries. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE This option is for persons affiliated with a CITI Program subscriber organization. To find your organization, enter its name in the box below, then pick from the list of choices provided. CLINICAL RESEARCH COORDINATOR (CRC) CRC courses provide foundational and advanced role-based training for clinical research professionals. The courses cover information that expands beyond but is directly connected to the Human Subjects Research (HSR) and Good Clinical Practice (GCP) courses. The Foundations course delivers basic CRC training that organizations may use for onboarding new CRCs. HUMAN SUBJECTS RESEARCH (HSR) Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE).They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards(IRBs).
CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. To register for independent learner courses, please contact n2@n2canada.ca. DECENTRALIZED CLINICAL TRIALS (DCTS) AND YOUR WORKFORCE Decentralized Clinical Trials (DCTs) and Your Workforce Explores changes to the site’s workforce including updates to traditional roles and new positions and WHAT CITI PROGRAM IS READING This week we're reading about EDPS investigations, a potential antiviral drug for COVID-19, language processing and AI research, the President's new science adviser, facilities adopting GMP, emerging tech trends for higher ed, and more.NEW WEBINAR
Add this webinar to your organization’s subscription. Learn more about this webinar . Description. With the current/recent global pandemic, many clinical trial sites had to adopt technology and adapt processes to allow remote work. REGISTER NOW: PRIVACY AND ETHICAL CONSIDERATIONS FOR This webinar provides an overview of what makes CAVs different from the cars of yesteryear, an overview of privacy and ethics, and an overview of the privacy and ethical challenges raised by CAVs. RESEARCH, ETHICS, AND COMPLIANCE TRAINING The Trusted Standard in Research, Ethics, and Compliance Training The Collaborative Institutional Training Initiative (CITI Program) is dedicated to serving the training needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - Collaborative Institutional Training Initiative. English Español Português 한국어 中文 Русский Français Tiếng Việt. New to the CITI Program? Read the getting started guide or CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. Use this option if you are paying for your courses. This option is for persons not affiliated with a CITI Program subscriber organization, or who require content that their organization does not provide. Fees apply. Credit card payment with American Express, Discover, MasterCard or Visa is required.Checks are
EXPLORE OUR COURSES
CITI Program offers research, ethics, and compliance training courses, as well as CME/CEU certified courses for a wide range of industries. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE We use cookies and other tracking technologies to recognize your repeat visits and preferences, as well as to analyze traffic and measure the effectiveness of communications. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVECITI COLLABORATIVE INSTITUTIONAL TRAINING INITIAT…CITI COLLABORATIVE INSTITUTIONAL TRAININGCITI TRAINING IRBCITI TRAINING LOGINCITI TRAINING PROGRAMCITI PROGRAM TRAINING CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. To register for independent learner courses, please contact n2@n2canada.ca. GOOD CLINICAL PRACTICE (GCP) Good Clinical Practice (GCP) includes basic courses tailored to the different types of clinical research. These courses also include corresponding refresher courses for retraining and advanced learning. CITI Program GCP training is used by over 1,500 institutions - (including many leading hospitals, academic medical centers,universities, and
HUMAN SUBJECTS RESEARCH (HSR) Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE).They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards(IRBs).
RESEARCH, ETHICS, AND COMPLIANCE TRAINING The Trusted Standard in Research, Ethics, and Compliance Training The Collaborative Institutional Training Initiative (CITI Program) is dedicated to serving the training needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - Collaborative Institutional Training Initiative. English Español Português 한국어 中文 Русский Français Tiếng Việt. New to the CITI Program? Read the getting started guide or CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. Use this option if you are paying for your courses. This option is for persons not affiliated with a CITI Program subscriber organization, or who require content that their organization does not provide. Fees apply. Credit card payment with American Express, Discover, MasterCard or Visa is required.Checks are
EXPLORE OUR COURSES
CITI Program offers research, ethics, and compliance training courses, as well as CME/CEU certified courses for a wide range of industries. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE We use cookies and other tracking technologies to recognize your repeat visits and preferences, as well as to analyze traffic and measure the effectiveness of communications. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVECITI COLLABORATIVE INSTITUTIONAL TRAINING INITIAT…CITI COLLABORATIVE INSTITUTIONAL TRAININGCITI TRAINING IRBCITI TRAINING LOGINCITI TRAINING PROGRAMCITI PROGRAM TRAINING CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. To register for independent learner courses, please contact n2@n2canada.ca. GOOD CLINICAL PRACTICE (GCP) Good Clinical Practice (GCP) includes basic courses tailored to the different types of clinical research. These courses also include corresponding refresher courses for retraining and advanced learning. CITI Program GCP training is used by over 1,500 institutions - (including many leading hospitals, academic medical centers,universities, and
HUMAN SUBJECTS RESEARCH (HSR) Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE).They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards(IRBs).
CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE GUIDE TO GETTING STARTED The Profiles Page is divided into 2 sections; Member Profile includes the information on your CITI Program account. To access your Member Profile information click on the View or Edit link. The Institutional Profiles contains information that was requested by the institution sponsoring your course access.These information fields are customizedper institution.
RADIATION SAFETY
This module introduces the fundamentals of radiation and more specifically, radioactive materials. Working with, or near, radioactive materials requires a familiarity with some basic concepts to better understand how to perform this work safely. CLINICAL RESEARCH COORDINATOR (CRC) CRC courses provide foundational and advanced role-based training for clinical research professionals. The courses cover information that expands beyond but is directly connected to the Human Subjects Research (HSR) and Good Clinical Practice (GCP) courses. The Foundations course delivers basic CRC training that organizations may use for onboarding new CRCs."FREE COURSES"
We use cookies and other tracking technologies to recognize your repeat visits and preferences, as well as to analyze traffic and measure the effectiveness of communications. HUMAN SUBJECTS RESEARCH (HSR) Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE).They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards(IRBs).
BIOSAFETY AND BIOSECURITY (BSS) BSS courses cover a variety of biosafety and biosecurity topics that address multiple regulations, standards, and guidelines. They are intended to complement the hands-on training and experience that those handling biohazards obtain from their principal investigators, laboratory managers, and SHARING COMPLETION CERTIFICATES AND COMPLETION REPORTS Completion Reports. Completion Reports are transcripts of your course work, and include all quiz scores. Part 1 shows scores "frozen" at the time you completed and passed the course. Part 2 reflects scores for any subsequent quiz attempts. Completion Reports may be used for TransCelerate mutual recognition. SHIPPING AND TRANSPORT OF REGULATED BIOLOGICAL MATERIALS Shipping and Transport of Regulated Biological Materials is designed as initial training and periodic retraining for employees who package or ship diagnostic and clinical human or animal specimens, human or animal pathogens, and other regulated biohazards. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - Collaborative Institutional Training Initiative. Thank you. The username (s) associated with your email address have been sent to your primary and secondary email addresses on file. RESEARCH, ETHICS, AND COMPLIANCE TRAINING The Trusted Standard in Research, Ethics, and Compliance Training The Collaborative Institutional Training Initiative (CITI Program) is dedicated to serving the training needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - Collaborative Institutional Training Initiative. English Español Português 한국어 中文 Русский Français Tiếng Việt. New to the CITI Program? Read the getting started guide or CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. Use this option if you are paying for your courses. This option is for persons not affiliated with a CITI Program subscriber organization, or who require content that their organization does not provide. Fees apply. Credit card payment with American Express, Discover, MasterCard or Visa is required.Checks are
EXPLORE OUR COURSES
CITI Program offers research, ethics, and compliance training courses, as well as CME/CEU certified courses for a wide range of industries. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE We use cookies and other tracking technologies to recognize your repeat visits and preferences, as well as to analyze traffic and measure the effectiveness of communications. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVECITI COLLABORATIVE INSTITUTIONAL TRAINING INITIAT…CITI COLLABORATIVE INSTITUTIONAL TRAININGCITI TRAINING IRBCITI TRAINING LOGINCITI TRAINING PROGRAMCITI PROGRAM TRAINING CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. To register for independent learner courses, please contact n2@n2canada.ca. GOOD CLINICAL PRACTICE (GCP) Good Clinical Practice (GCP) includes basic courses tailored to the different types of clinical research. These courses also include corresponding refresher courses for retraining and advanced learning. CITI Program GCP training is used by over 1,500 institutions - (including many leading hospitals, academic medical centers,universities, and
HUMAN SUBJECTS RESEARCH (HSR) Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE).They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards(IRBs).
RESEARCH, ETHICS, AND COMPLIANCE TRAINING The Trusted Standard in Research, Ethics, and Compliance Training The Collaborative Institutional Training Initiative (CITI Program) is dedicated to serving the training needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - Collaborative Institutional Training Initiative. English Español Português 한국어 中文 Русский Français Tiếng Việt. New to the CITI Program? Read the getting started guide or CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. Use this option if you are paying for your courses. This option is for persons not affiliated with a CITI Program subscriber organization, or who require content that their organization does not provide. Fees apply. Credit card payment with American Express, Discover, MasterCard or Visa is required.Checks are
EXPLORE OUR COURSES
CITI Program offers research, ethics, and compliance training courses, as well as CME/CEU certified courses for a wide range of industries. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE We use cookies and other tracking technologies to recognize your repeat visits and preferences, as well as to analyze traffic and measure the effectiveness of communications. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVECITI COLLABORATIVE INSTITUTIONAL TRAINING INITIAT…CITI COLLABORATIVE INSTITUTIONAL TRAININGCITI TRAINING IRBCITI TRAINING LOGINCITI TRAINING PROGRAMCITI PROGRAM TRAINING CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. To register for independent learner courses, please contact n2@n2canada.ca. GOOD CLINICAL PRACTICE (GCP) Good Clinical Practice (GCP) includes basic courses tailored to the different types of clinical research. These courses also include corresponding refresher courses for retraining and advanced learning. CITI Program GCP training is used by over 1,500 institutions - (including many leading hospitals, academic medical centers,universities, and
HUMAN SUBJECTS RESEARCH (HSR) Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE).They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards(IRBs).
CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE GUIDE TO GETTING STARTED The Profiles Page is divided into 2 sections; Member Profile includes the information on your CITI Program account. To access your Member Profile information click on the View or Edit link. The Institutional Profiles contains information that was requested by the institution sponsoring your course access.These information fields are customizedper institution.
RADIATION SAFETY
This module introduces the fundamentals of radiation and more specifically, radioactive materials. Working with, or near, radioactive materials requires a familiarity with some basic concepts to better understand how to perform this work safely. CLINICAL RESEARCH COORDINATOR (CRC) CRC courses provide foundational and advanced role-based training for clinical research professionals. The courses cover information that expands beyond but is directly connected to the Human Subjects Research (HSR) and Good Clinical Practice (GCP) courses. The Foundations course delivers basic CRC training that organizations may use for onboarding new CRCs."FREE COURSES"
We use cookies and other tracking technologies to recognize your repeat visits and preferences, as well as to analyze traffic and measure the effectiveness of communications. HUMAN SUBJECTS RESEARCH (HSR) Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE).They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards(IRBs).
BIOSAFETY AND BIOSECURITY (BSS) BSS courses cover a variety of biosafety and biosecurity topics that address multiple regulations, standards, and guidelines. They are intended to complement the hands-on training and experience that those handling biohazards obtain from their principal investigators, laboratory managers, and SHARING COMPLETION CERTIFICATES AND COMPLETION REPORTS Completion Reports. Completion Reports are transcripts of your course work, and include all quiz scores. Part 1 shows scores "frozen" at the time you completed and passed the course. Part 2 reflects scores for any subsequent quiz attempts. Completion Reports may be used for TransCelerate mutual recognition. SHIPPING AND TRANSPORT OF REGULATED BIOLOGICAL MATERIALS Shipping and Transport of Regulated Biological Materials is designed as initial training and periodic retraining for employees who package or ship diagnostic and clinical human or animal specimens, human or animal pathogens, and other regulated biohazards. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - Collaborative Institutional Training Initiative. Thank you. The username (s) associated with your email address have been sent to your primary and secondary email addresses on file. RESEARCH, ETHICS, AND COMPLIANCE TRAINING The Trusted Standard in Research, Ethics, and Compliance Training The Collaborative Institutional Training Initiative (CITI Program) is dedicated to serving the training needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - Collaborative Institutional Training Initiative. English Español Português 한국어 中文 Русский Français Tiếng Việt. New to the CITI Program? Read the getting started guide or CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. Use this option if you are paying for your courses. This option is for persons not affiliated with a CITI Program subscriber organization, or who require content that their organization does not provide. Fees apply. Credit card payment with American Express, Discover, MasterCard or Visa is required.Checks are
EXPLORE OUR COURSES
CITI Program offers research, ethics, and compliance training courses, as well as CME/CEU certified courses for a wide range of industries. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE We use cookies and other tracking technologies to recognize your repeat visits and preferences, as well as to analyze traffic and measure the effectiveness of communications. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVECITI COLLABORATIVE INSTITUTIONAL TRAINING INITIAT…CITI COLLABORATIVE INSTITUTIONAL TRAININGCITI TRAINING IRBCITI TRAINING LOGINCITI TRAINING PROGRAMCITI PROGRAM TRAINING CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. To register for independent learner courses, please contact n2@n2canada.ca. GOOD CLINICAL PRACTICE (GCP) Good Clinical Practice (GCP) includes basic courses tailored to the different types of clinical research. These courses also include corresponding refresher courses for retraining and advanced learning. CITI Program GCP training is used by over 1,500 institutions - (including many leading hospitals, academic medical centers,universities, and
HUMAN SUBJECTS RESEARCH (HSR) Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE).They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards(IRBs).
RESEARCH, ETHICS, AND COMPLIANCE TRAINING The Trusted Standard in Research, Ethics, and Compliance Training The Collaborative Institutional Training Initiative (CITI Program) is dedicated to serving the training needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - Collaborative Institutional Training Initiative. English Español Português 한국어 中文 Русский Français Tiếng Việt. New to the CITI Program? Read the getting started guide or CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. Use this option if you are paying for your courses. This option is for persons not affiliated with a CITI Program subscriber organization, or who require content that their organization does not provide. Fees apply. Credit card payment with American Express, Discover, MasterCard or Visa is required.Checks are
EXPLORE OUR COURSES
CITI Program offers research, ethics, and compliance training courses, as well as CME/CEU certified courses for a wide range of industries. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE We use cookies and other tracking technologies to recognize your repeat visits and preferences, as well as to analyze traffic and measure the effectiveness of communications. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVECITI COLLABORATIVE INSTITUTIONAL TRAINING INITIAT…CITI COLLABORATIVE INSTITUTIONAL TRAININGCITI TRAINING IRBCITI TRAINING LOGINCITI TRAINING PROGRAMCITI PROGRAM TRAINING CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE Independent Learner Registration. To register for independent learner courses, please contact n2@n2canada.ca. GOOD CLINICAL PRACTICE (GCP) Good Clinical Practice (GCP) includes basic courses tailored to the different types of clinical research. These courses also include corresponding refresher courses for retraining and advanced learning. CITI Program GCP training is used by over 1,500 institutions - (including many leading hospitals, academic medical centers,universities, and
HUMAN SUBJECTS RESEARCH (HSR) Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE).They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards(IRBs).
CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE GUIDE TO GETTING STARTED The Profiles Page is divided into 2 sections; Member Profile includes the information on your CITI Program account. To access your Member Profile information click on the View or Edit link. The Institutional Profiles contains information that was requested by the institution sponsoring your course access.These information fields are customizedper institution.
RADIATION SAFETY
This module introduces the fundamentals of radiation and more specifically, radioactive materials. Working with, or near, radioactive materials requires a familiarity with some basic concepts to better understand how to perform this work safely. CLINICAL RESEARCH COORDINATOR (CRC) CRC courses provide foundational and advanced role-based training for clinical research professionals. The courses cover information that expands beyond but is directly connected to the Human Subjects Research (HSR) and Good Clinical Practice (GCP) courses. The Foundations course delivers basic CRC training that organizations may use for onboarding new CRCs."FREE COURSES"
We use cookies and other tracking technologies to recognize your repeat visits and preferences, as well as to analyze traffic and measure the effectiveness of communications. HUMAN SUBJECTS RESEARCH (HSR) Human Subjects Research (HSR) content is organized into two tracks: Biomedical (Biomed) and Social-Behavioral-Educational (SBE).They are intended for anyone involved in research studies with human subjects, or who have responsibilities for setting policies and procedures with respect to such research, including Institutional Review Boards(IRBs).
BIOSAFETY AND BIOSECURITY (BSS) BSS courses cover a variety of biosafety and biosecurity topics that address multiple regulations, standards, and guidelines. They are intended to complement the hands-on training and experience that those handling biohazards obtain from their principal investigators, laboratory managers, and SHARING COMPLETION CERTIFICATES AND COMPLETION REPORTS Completion Reports. Completion Reports are transcripts of your course work, and include all quiz scores. Part 1 shows scores "frozen" at the time you completed and passed the course. Part 2 reflects scores for any subsequent quiz attempts. Completion Reports may be used for TransCelerate mutual recognition. SHIPPING AND TRANSPORT OF REGULATED BIOLOGICAL MATERIALS Shipping and Transport of Regulated Biological Materials is designed as initial training and periodic retraining for employees who package or ship diagnostic and clinical human or animal specimens, human or animal pathogens, and other regulated biohazards. CITI - COLLABORATIVE INSTITUTIONAL TRAINING INITIATIVE CITI - Collaborative Institutional Training Initiative. Thank you. The username (s) associated with your email address have been sent to your primary and secondary email addresses on file.Skip Navigation
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The Trusted Standard in Research, Ethics, and Compliance Training The Collaborative Institutional Training Initiative (CITI Program) is dedicated to serving the training needs of colleges and universities, healthcare institutions, technology and research organizations, and governmental agencies, as they foster integrity and professional advancement of their learners.Demo a Course
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Over 10 Million Course Completions Celebrating 20 Years of Serving the Research Community Utilized by the Top-25 Best National Universities** 1
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EXPLORE OUR COURSE CATALOG* What's New
* Research
* Ethics
* Compliance
* Professional
Previous
CONFLICT MANAGEMENT
New
Provides an overview of conflict, types of conflict, conflict styles, communication styles, and intervention strategies.view course
TECHNOLOGY TRANSFER
New
An introduction for researchers on university technology transfer and commercialization processes.view course
TEACHING AND TRAINING FOR PROFESSIONALSNew
Provides instruction on how to improve your teaching and training skills in a variety of settings.view course
IMPORTANCE OF PEER REVIEW AND DATA VALIDATION IN RESEARCHNew
This webinar covers the types, limits, and ethical guidelines of peer review along with federal regulations and criteria for evaluatingproposals.
view webinar
view series
FERPA AND ONLINE LEARNING IN THE TIME OF COVID-19New
This webinar covers student data privacy issues with online learning including compliance with FERPA and other regulations.view webinar
view series
WORKING WITH YOUR IRBNew
Strategies to work with your reviewing IRB.view webinar
view
series
PARTICIPATING IN VACCINE RESEARCH (FREE WEBINAR)New
Learn about what to expect when participating in vaccine research.view webinar
view series
COVID-19 AND HUMAN RESEARCH PROTECTION PROGRAMSNew
This webinar reviews how a human research protection program (HRPP) responded to and dealt with the COVID-19 pandemic.view webinar
view series
SOCIAL MEDIA AND RESEARCH RECRUITINGNew
Discusses social media use in research recruiting.view webinar
view series
ARTIFICIAL INTELLIGENCE (AI) AND HUMAN SUBJECT PROTECTIONSNew
Explores the current protections, regulatory elements, and ethics tools associated with protecting human subjects in light of AIresearch.
view webinar
view series
NUTS & BOLTS OF RUNNING A VIRTUAL IRB MEETINGNew
Explores aspects of virtual IRB meetings including the benefits, tech setup, documentation, and more particularly during a disaster.view webinar
view series
COVID-19: INSIGHTS FOR HIGHER ED LEADERS (FREE COURSE)New
Gain insights to guide strategic planning surrounding COVID-19 operations in Higher Ed.view course
view series
ACCREDITATION 101 FOR NEW AND ADJUNCT FACULTYNew
Learn about the importance of accreditation and the role you may plan in your institution’s annual accreditation renewal process.view webinar
view series
TITLE IX AND THE NEW REGULATIONSNew
Discusses key elements of the new 2020 regulations, how they affect the institutional community, and what you should know to implement best practices into revised Title IX procedures and policies.view webinar
view series
INTERNATIONAL STUDENTS IN U.S. HIGHER EDNew
Discusses different visa types pertaining to international students and their effect on student activities on and off campus.view webinar
view series
REMOTE CONTACT TRACING(FREE COURSE)
New
Train individuals to conduct remote contact tracing for COVID-19 according to an established protocol and using evidence-basedpractices.
view course
view
series
INFORMED CONSENT AND CLINICAL INVESTIGATIONS: A FOCUS ON THE PROCESSNew
Explores current challenges and improvement strategies related toinformed consent.
view webinar
view series
EXPORT COMPLIANCE: AN OVERVIEW FOR STAFF, STUDENTS, AND FACULTYNew
Provides faculty, staff, and students with an overview of U.S. export control regulations and their application to various activities within institutions of higher education.view webinar
view series
COVID-19: ETHICAL CARE AND WORKFORCE CONCERNSNew
Reviews public health duties, resources challenges, workforce response, and collaborating with regional hospitals.view webinar
view series
FALSE CLAIMS ACT: A PRIMER AND GUIDE FOR RESEARCH ORGANIZATIONSNew
This course provides an introduction to the False Claims Act ideally suited for faculty, researchers, and staff at research organizations.view course
FDA INSPECTIONS: FROM SITE PREPARATION TO RESPONSENew
Covers regulatory inspections of clinical investigators and sites, including mock inspections, 482s, 483s, warning letters, communication, and CAPA plans.view course
COVID-19: BACK TO CAMPUS (2020-2021)New
A complimentary course to train staff, students, and faculty on COVID-19 safety for their return to campus.view course
GDPR FOR RESEARCH AND HIGHER EDNew
Overview of the European Union’s (EU) General Data ProtectionRegulation (GDPR).
view course
TECHNOLOGY, ETHICS, AND REGULATIONSNewUpdated
Covers various technologies and their associated ethical issues and governance approaches.view course
UNDUE FOREIGN INFLUENCE: RISKS AND MITIGATIONSNew
Explore key ethical, export, security, intellectual property, and transparency requirements related to international engagement.view course
CONFLICT MANAGEMENT
New
Provides an overview of conflict, types of conflict, conflict styles, communication styles, and intervention strategies.view course
TECHNOLOGY TRANSFER
New
An introduction for researchers on university technology transfer and commercialization processes.view course
TEACHING AND TRAINING FOR PROFESSIONALSNew
Provides instruction on how to improve your teaching and training skills in a variety of settings.view course
IMPORTANCE OF PEER REVIEW AND DATA VALIDATION IN RESEARCHNew
This webinar covers the types, limits, and ethical guidelines of peer review along with federal regulations and criteria for evaluatingproposals.
view webinar
view series
FERPA AND ONLINE LEARNING IN THE TIME OF COVID-19New
This webinar covers student data privacy issues with online learning including compliance with FERPA and other regulations.view webinar
view series
WORKING WITH YOUR IRBNew
Strategies to work with your reviewing IRB.view webinar
view
series Next
Previous
FDA INSPECTIONS: FROM SITE PREPARATION TO RESPONSENew
Covers regulatory inspections of clinical investigators and sites, including mock inspections, 482s, 483s, warning letters, communication, and CAPA plans.view course
UNDUE FOREIGN INFLUENCE: RISKS AND MITIGATIONSNew
Explore key ethical, export, security, intellectual property, and transparency requirements related to international engagement.view course
TECHNOLOGY TRANSFER
New
An introduction for researchers on university technology transfer and commercialization processes.view course
CLINICAL RESEARCH COORDINATOR (CRC) FOUNDATIONSCME/CEU
This course provides basic CRC training.view course
view series
DISASTER PLANNING FOR THE RESEARCH ENTERPRISEFeatured
This course offers information about disaster planning and business continuity to those responsible for research oversight.view course
INSTITUTIONAL REVIEW BOARD (IRB) ADMINISTRATIONCME/CEU
This course offers a comprehensive review of the critical areas associated with IRB and IRB office operations.view course
GCP FOR CLINICAL INVESTIGATIONS OF DRUGS AND BIOLOGICS (ICH)CME/CEU
Ideal for individuals proposing to conduct clinical trials of drugs and biologics in the U.S. or internationally.view course
view series
GCP FOR CLINICAL INVESTIGATIONS OF DRUGS AND DEVICES (FDA)CME/CEU
Ideal for individuals proposing to conduct clinical trials of drugs, biologics, and devices primarily in the U.S.view course
view series
ESSENTIALS OF RESEARCH ADMINISTRATIONCME/CEU
This course provides an overview of research administration.view course
CLINICAL TRIAL BILLING COMPLIANCE (CTBC)CME/CEU
This course focuses on developing the knowledge and skills necessary to maintain compliance and best practices associated with clinicalresearch billing.
view course
SOCIAL-BEHAVIORAL-EDUCATIONAL (SBE) BASICCME/CEU
This course covers the core human subjects research topics for social-behavioral-educational researchers.view course
view series
CLINICALTRIALS.GOV: PROTOCOL REGISTRATION & RESULTS DISCLOSUREFeatured
A video-enhanced guide to compliance with the FDAAA Final Rule and NIH Policy on clinical trial disclosure.view
course
BIOMEDICAL PRINCIPAL INVESTIGATORCME/CEU
This role-based course covers supervision, delegation, management, reports, and communication for investigators.view course
WORKING WITH YOUR IRBNew
Strategies to work with your reviewing IRB.view webinar
view
series
PARTICIPATING IN VACCINE RESEARCH (FREE WEBINAR)New
Learn about what to expect when participating in vaccine research.view webinar
view series
INFORMED CONSENT AND CLINICAL INVESTIGATIONS: A FOCUS ON THE PROCESSNew
Explores current challenges and improvement strategies related toinformed consent.
view webinar
view series
BIOMEDICAL (BIOMED) BASICCME/CEU
This course covers the core human subjects research topics for biomedical researchers.view course
view series
FDA INSPECTIONS: FROM SITE PREPARATION TO RESPONSENew
Covers regulatory inspections of clinical investigators and sites, including mock inspections, 482s, 483s, warning letters, communication, and CAPA plans.view course
UNDUE FOREIGN INFLUENCE: RISKS AND MITIGATIONSNew
Explore key ethical, export, security, intellectual property, and transparency requirements related to international engagement.view course
TECHNOLOGY TRANSFER
New
An introduction for researchers on university technology transfer and commercialization processes.view course
CLINICAL RESEARCH COORDINATOR (CRC) FOUNDATIONSCME/CEU
This course provides basic CRC training.view course
view series
DISASTER PLANNING FOR THE RESEARCH ENTERPRISEFeatured
This course offers information about disaster planning and business continuity to those responsible for research oversight.view course
INSTITUTIONAL REVIEW BOARD (IRB) ADMINISTRATIONCME/CEU
This course offers a comprehensive review of the critical areas associated with IRB and IRB office operations.view course
Next
Previous
FALSE CLAIMS ACT: A PRIMER AND GUIDE FOR RESEARCH ORGANIZATIONSNew
This course provides an introduction to the False Claims Act ideally suited for faculty, researchers, and staff at research organizations.view course
GDPR FOR RESEARCH AND HIGHER EDNew
Overview of the European Union’s (EU) General Data ProtectionRegulation (GDPR).
view course
TECHNOLOGY, ETHICS, AND REGULATIONSNewUpdated
Covers various technologies and their associated ethical issues and governance approaches.view course
HEALTHCARE ETHICS COMMITTEE (HEC)CME/CEU
This course focuses on developing the knowledge and skill base necessary for being a successful healthcare ethics committee member.view course
FAMILY EDUCATIONAL RIGHTS AND PRIVACY ACT (FERPA)CME/CEU
This course covers the core requirements of the federal Family Educational Rights and Privacy Act (FERPA).view course
view series
CONFLICTS OF INTEREST (COI) BASICCME/CEU
This course provides foundational training on the PHS regulations associated with financial conflicts of interests.view course
view series
INFORMATION SECURITYCME/CEU
This course provides information on basic techniques for data and device security, including email and mobile devices.view course
view
series
HEALTH PRIVACY (HIPAA)CME/CEU
This course is intended to cover the core elements of the federal Health Insurance Portability and Accountability Act (HIPAA)requirements.
view course
view series
BIOETHICS
CME/CEU
This course provides learners with a review of contemporary bioethicsissues.
view course
ARTIFICIAL INTELLIGENCE (AI) AND HUMAN SUBJECT PROTECTIONSNew
Explores the current protections, regulatory elements, and ethics tools associated with protecting human subjects in light of AIresearch.
view webinar
view series
ETHICS & POLICY ISSUES IN CRISPR GENE EDITINGFeatured
Explore the ethical and policy issues that CRISPR gene editing presents in this engaging webinar.view webinar
view series
COMPENSATION REPORTING (EFFORT REPORTING)Featured
A focused discussion for individuals who work with federally sponsored awards, PIs, and other members of the research team.view course
FALSE CLAIMS ACT: A PRIMER AND GUIDE FOR RESEARCH ORGANIZATIONSNew
This course provides an introduction to the False Claims Act ideally suited for faculty, researchers, and staff at research organizations.view course
GDPR FOR RESEARCH AND HIGHER EDNew
Overview of the European Union’s (EU) General Data ProtectionRegulation (GDPR).
view course
TECHNOLOGY, ETHICS, AND REGULATIONSNewUpdated
Covers various technologies and their associated ethical issues and governance approaches.view course
HEALTHCARE ETHICS COMMITTEE (HEC)CME/CEU
This course focuses on developing the knowledge and skill base necessary for being a successful healthcare ethics committee member.view course
FAMILY EDUCATIONAL RIGHTS AND PRIVACY ACT (FERPA)CME/CEU
This course covers the core requirements of the federal Family Educational Rights and Privacy Act (FERPA).view course
view series
CONFLICTS OF INTEREST (COI) BASICCME/CEU
This course provides foundational training on the PHS regulations associated with financial conflicts of interests.view course
view series
Next
Previous
EXPORT COMPLIANCE: AN OVERVIEW FOR STAFF, STUDENTS, AND FACULTYNew
Provides faculty, staff, and students with an overview of U.S. export control regulations and their application to various activities within institutions of higher education.view webinar
view series
BIOMEDICAL (BIOMED) BASICCME/CEU
This course covers the core human subjects research topics for biomedical researchers.view course
view series
GDPR FOR RESEARCH AND HIGHER EDNew
Overview of the European Union’s (EU) General Data ProtectionRegulation (GDPR).
view course
RESPONSIBLE CONDUCT OF RESEARCH (RCR) BASICCME/CEU
This course covers the core norms, principles, regulations, and rules governing the practice of research.view course
view series
EXPORT COMPLIANCE (EC) BASICCME/CEU
This course provides an overview of export compliance regulations along with information specifically tailored for certain roles andresponsibilities.
view course
view
series
WORKING WITH GENETICALLY MODIFIED MICE IN RESEARCH SETTINGSFeatured
This course provides training on working with genetically modified mice in research settings.view course
view series
WORKING WITH THE IACUCFeatured
This course provides basic training on the protection of animal subjects used in research.view course
view
series
HEALTH PRIVACY (HIPAA)CME/CEU
This course is intended to cover the core elements of the federal Health Insurance Portability and Accountability Act (HIPAA)requirements.
view course
view series
SOCIAL-BEHAVIORAL-EDUCATIONAL (SBE) BASICCME/CEU
This course covers the core human subjects research topics for social-behavioral-educational researchers.view course
view series
CLINICALTRIALS.GOV: PROTOCOL REGISTRATION & RESULTS DISCLOSUREFeatured
A video-enhanced guide to compliance with the FDAAA Final Rule and NIH Policy on clinical trial disclosure.view
course
SEMIANNUAL EVALUATIONS IN DEPTHFeatured
This course provides IACUC members and administrators with more in-depth information about the conduct of semiannual evaluations.view course
INITIAL BIOSAFETY TRAININGCME/CEU
This course offers initial training for researchers handling biohazards in a research or clinical laboratory.view course
view series
LABORATORY CHEMICAL SAFETYFeatured
This course covers the fundamental safety practices for working with hazardous chemicals in the laboratory.view course
WORKING WITH YOUR IRBNew
Strategies to work with your reviewing IRB.view webinar
view
series
PARTICIPATING IN VACCINE RESEARCH (FREE WEBINAR)New
Learn about what to expect when participating in vaccine research.view webinar
view series
COVID-19: INSIGHTS FOR HIGHER ED LEADERS (FREE COURSE)New
Gain insights to guide strategic planning surrounding COVID-19 operations in Higher Ed.view course
view series
ACCREDITATION 101 FOR NEW AND ADJUNCT FACULTYNew
Learn about the importance of accreditation and the role you may plan in your institution’s annual accreditation renewal process.view webinar
view series
TITLE IX AND THE NEW REGULATIONSNew
Discusses key elements of the new 2020 regulations, how they affect the institutional community, and what you should know to implement best practices into revised Title IX procedures and policies.view webinar
view series
INFORMED CONSENT AND CLINICAL INVESTIGATIONS: A FOCUS ON THE PROCESSNew
Explores current challenges and improvement strategies related toinformed consent.
view webinar
view series
EXPORT COMPLIANCE: AN OVERVIEW FOR STAFF, STUDENTS, AND FACULTYNew
Provides faculty, staff, and students with an overview of U.S. export control regulations and their application to various activities within institutions of higher education.view webinar
view series
BIOMEDICAL (BIOMED) BASICCME/CEU
This course covers the core human subjects research topics for biomedical researchers.view course
view series
GDPR FOR RESEARCH AND HIGHER EDNew
Overview of the European Union’s (EU) General Data ProtectionRegulation (GDPR).
view course
RESPONSIBLE CONDUCT OF RESEARCH (RCR) BASICCME/CEU
This course covers the core norms, principles, regulations, and rules governing the practice of research.view course
view series
EXPORT COMPLIANCE (EC) BASICCME/CEU
This course provides an overview of export compliance regulations along with information specifically tailored for certain roles andresponsibilities.
view course
view
series
WORKING WITH GENETICALLY MODIFIED MICE IN RESEARCH SETTINGSFeatured
This course provides training on working with genetically modified mice in research settings.view course
view series
Next
Previous
REMOTE CONTACT TRACING(FREE COURSE)
New
Train individuals to conduct remote contact tracing for COVID-19 according to an established protocol and using evidence-basedpractices.
view course
view
series
CONFLICT MANAGEMENT
New
Provides an overview of conflict, types of conflict, conflict styles, communication styles, and intervention strategies.view course
TEACHING AND TRAINING FOR PROFESSIONALSNew
Provides instruction on how to improve your teaching and training skills in a variety of settings.view course
ESSENTIALS OF RESEARCH ADMINISTRATIONCME/CEU
This course provides an overview of research administration.view course
INSTITUTIONAL/SIGNATORY OFFICIAL: HUMAN SUBJECTS RESEARCHFeatured
Provides a foundational training for institutional/signatory officials on their roles and responsibilities as part of an HRPP.view course
view series
INSTITUTIONAL REVIEW BOARD (IRB) CHAIRCME/CEU
This course provides detailed training for current and future Institutional Review Board (IRB) chairs.view course
view
series
CLINICAL RESEARCH COORDINATOR (CRC) ADVANCEDCME/CEU
This course provides clinical research professionals with advanced training tailored to the CRC’s critical role in the conduct ofclinical trials.
view course
view series
RESEARCH STUDY DESIGNFeatured
This course provides learners with an understanding of how to improve study design, collect and analyze data, and promote reproducibleresearch.
view course
ESSENTIALS OF STATISTICAL ANALYSIS: COMPLETE (PARTS 1, 2, AND 3)Featured
Teaches learners the essentials of statistical analysis.view course
view series
ESSENTIALS OF GRANT PROPOSAL DEVELOPMENTCME/CEU
This course provides a step-by-step guide to help simplify the grantwriting process.
view course
IACUC ADMINISTRATIONFeatured
This course provides a comprehensive review of IACUC administration, including the IACUC administrator’s specific roles and responsibilities in an animal care and use program.view course
BIOSAFETY OFFICER TRAINING – BASICFeatured
This course offers an Introduction to biosafety for new biosafety officers and other environmental health and safety professionals.view course
view series
SOCIAL MEDIA AND RESEARCH RECRUITINGNew
Discusses social media use in research recruiting.view webinar
view series
MEDICAL MARIJUANA: A BUDDING FIELD OF RESEARCHFeatured
Discuss unique challenges and issues as well as considerations for IRB review and steps for getting started in medical marijuana research.view webinar
view series
RUNNING A VIRTUAL IRB MEETINGFeatured
Explore different elements associated with running an IRB meeting in a virtual environment, including key areas for IRB chairs, members, andstaff.
view webinar
view series
ACCREDITATION 101 FOR NEW AND ADJUNCT FACULTYNew
Learn about the importance of accreditation and the role you may plan in your institution’s annual accreditation renewal process.view webinar
view series
INTERNATIONAL STUDENTS IN U.S. HIGHER EDNew
Discusses different visa types pertaining to international students and their effect on student activities on and off campus.view webinar
view series
REMOTE CONTACT TRACING(FREE COURSE)
New
Train individuals to conduct remote contact tracing for COVID-19 according to an established protocol and using evidence-basedpractices.
view course
view
series
CONFLICT MANAGEMENT
New
Provides an overview of conflict, types of conflict, conflict styles, communication styles, and intervention strategies.view course
TEACHING AND TRAINING FOR PROFESSIONALSNew
Provides instruction on how to improve your teaching and training skills in a variety of settings.view course
ESSENTIALS OF RESEARCH ADMINISTRATIONCME/CEU
This course provides an overview of research administration.view course
INSTITUTIONAL/SIGNATORY OFFICIAL: HUMAN SUBJECTS RESEARCHFeatured
Provides a foundational training for institutional/signatory officials on their roles and responsibilities as part of an HRPP.view course
view series
INSTITUTIONAL REVIEW BOARD (IRB) CHAIRCME/CEU
This course provides detailed training for current and future Institutional Review Board (IRB) chairs.view course
view
series
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JOIN OVER 2,000 SUBSCRIBING ORGANIZATIONS Highlighted below are just a few select subscribers & collaborators. Subscribing Organizations MEET A FEW OF OUR EXPERT AUTHORS AND PRESENTERS Our courses are built by over 150 highly qualified experts and rigorously peer reviewed to incorporate various perspectives and ensure accuracy, completeness, and overall quality.Previous
LAUREL LYCKHOLM, MD
University of Iowa Carver College of Medicine Dr. Lyckholm is a Hematologist /Oncologist and Palliative Care specialist. She is also trained in bioethics. Her primary interest is in provision of cancer and palliative care to underserved populations.Meet The Author
TRACY ARWOOD, MS
Clemson University
Ms. Tracy Arwood is currently the Chief Ethics & Compliance Officer at Clemson University. In this role, she manages an enterprise-wide compliance and ethics program that provides guidance and oversight with respect to the vast range of legal requirements affecting institutions of higher learning.Meet The Author
LORI MCDONALD, PHD
University of Utah
Lori McDonald, PhD, is currently serving as Vice President for Student Affairs at the University of Utah. McDonald earned her doctorate from the U in Educational Leadership & Policy. This year marks her twenty-fourth year serving within the division of Student Affairs at the University of Utah.Meet The Author
DENNIS CULHANE, PHD
University of Pennsylvania Dennis Culhane is the Dana and Andrew Stone Professor of Social Policy at the School of Social Policy and Practice at The University of Pennsylvania, and served as the Director of Research at the National Center on Homelessness among Veterans at the US Department of Veterans Affairs from 2009-2018.Meet The Author
LAUREL LYCKHOLM, MD
University of Iowa Carver College of Medicine Dr. Lyckholm is a Hematologist /Oncologist and Palliative Care specialist. She is also trained in bioethics. Her primary interest is in provision of cancer and palliative care to underserved populations.Meet The Author
TRACY ARWOOD, MS
Clemson University
Ms. Tracy Arwood is currently the Chief Ethics & Compliance Officer at Clemson University. In this role, she manages an enterprise-wide compliance and ethics program that provides guidance and oversight with respect to the vast range of legal requirements affecting institutions of higher learning.Meet The Author
LORI MCDONALD, PHD
University of Utah
Lori McDonald, PhD, is currently serving as Vice President for Student Affairs at the University of Utah. McDonald earned her doctorate from the U in Educational Leadership & Policy. This year marks her twenty-fourth year serving within the division of Student Affairs at the University of Utah.Meet The Author
DENNIS CULHANE, PHD
University of Pennsylvania Dennis Culhane is the Dana and Andrew Stone Professor of Social Policy at the School of Social Policy and Practice at The University of Pennsylvania, and served as the Director of Research at the National Center on Homelessness among Veterans at the US Department of Veterans Affairs from 2009-2018.Meet The Author
LAUREL LYCKHOLM, MD
University of Iowa Carver College of Medicine Dr. Lyckholm is a Hematologist /Oncologist and Palliative Care specialist. She is also trained in bioethics. Her primary interest is in provision of cancer and palliative care to underserved populations.Meet The Author
TRACY ARWOOD, MS
Clemson University
Ms. Tracy Arwood is currently the Chief Ethics & Compliance Officer at Clemson University. In this role, she manages an enterprise-wide compliance and ethics program that provides guidance and oversight with respect to the vast range of legal requirements affecting institutions of higher learning.Meet The Author
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Browse Authors and Presenters IN OUR LEARNERS' WORDSALI S.
PhD Candidate and Adjunct Faculty _“I could review, take the quiz, and receive feedback. Also, ease of access was great.”_JANET H.
Coordinator and Assistant Professor, School of InterdisciplinaryHealth Programs
_“The current version is more practical than the last time I took the training. I can apply all concepts to my research.”_ANGÉLICA M.
Clinical Research Coordinator, Specializing in HPV cancer prevention “I’m a fan of the revised formatting and pictographs. It allows me to choose how to receive the information, and promotes more engagementoverall.”
KRISTI W.
IRB Department Secretary _“The format, organization, and quizzes were very user-friendly. I appreciated the option to switch between the traditional and audio-visual formats because I could adapt to my needs at themoment.”_
COURSES APPROVED BY A TOP ACADEMIC CME PROVIDER CITI Program courses are approved for CME credits through the ALBERT EINSTEIN MONTEFIORE CONTINUING PROFESSIONAL DEVELOPMENT CENTER (CPDC). Albert Einstein College of Medicine-Montefiore Medical Center (Einstein) is accredited by the JOINT ACCREDITATION FOR INTERPROFESSIONAL CONTINUING EDUCATION to provide continuing education activities for healthcare professionals. Einstein is accredited to offer continuing education credit for the following professions: medicine, nursing and psychology. View CE Certified Courses LEARN ABOUT CITI PROGRAM See why so many organizations rely on CITI Program for efficient andeffective training.
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