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Description:Blog CIP Exam Preparation and Recertification Using CITI Program Content Study Help for the CIP Exam As the application deadline for the Fall 2020 CIP examination approaches 14 August for the exam window of 7 September through 7 October remember that CITI Program’s Human Subjects Research and IRB Administration courses can help you prepare

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Some functions of this CITI Program website will not work properly unless you upgrade your web browser. This site works best with latest versions of these browsers. NOTE: Your organization may have restrictions on installing new software on its computers. Know the rules at your organization before you download and install a new browser version. Login to CITI This CITI Program website will not work properly unless you upgrade your web browser. This site works best with latest versions of these browsers. NOTE: Your organization may have restrictions on installing new software on its computers. Know the rules at your organization before you download and install a new browser version. Skip Navigation +1 888.529.5929 English Español 한국어 Português 中文 Русский 日本語 français tiếng Việt Register Log In -- Español 한국어 Português 中文 Русский 日本語 français tiếng Việt -- +1 888.529.5929 Register Log In MENU MENU Subscriptions Organizational Subscriptions Setting Up CITI Program Learners: How to Take Courses CITI Program Advantages Courses View All CE Certified Courses Animal Care and Use (ACU) Bioethics Biomedical PI Biosafety and Biosecurity (BSS) Clinical Research Coordinator (CRC) Clinical Trial Billing Compliance (CTBC) Compensation Reporting Conflicts of Interest (COI) Disaster Planning for the Research Enterprise (DPRE) Essentials of Grant Proposal Development Essentials of Research Administration Essentials of Statistical Analysis (EOSA) Export Compliance (EC) Good Clinical Practice (GCP) Good Laboratory Practice (GLP) Healthcare Ethics Committee (HEC) Human Subjects Research (HSR) IACUC Administration Information Privacy & Security (IPS) IRB Administration Laboratory Chemical Safety Protocol Registration and Results Summary Disclosure in ClinicalTrials.gov Research Study Design Responsible Conduct of Research (RCR) Semiannual Evaluations In Depth Webinars View All Courses Tools Support Support Center FAQ Sales Center CE/CMEs Research Ethics and Compliance Training Compensation Reporting Explore the requirements of and compliance with compensation reporting on federal awards. View Course Running a Virtual IRB Meeting Identify strategies for running an IRB meeting in a virtual environment, addressing key areas for IRB chairs, members, and staff. View Webinar BRANY SBER IRB Services Social, behavioral, and educational research has its own set of unique needs, and we understand them. Find out more about the SBER expertise, experience, and unique connected model of our accredited IRB. Learn More Laboratory Chemical Safety Learn the fundamental safety practices for working with hazardous chemicals in the laboratory. View Course Understanding Consent Requirements and “Key Information” Under the Revised Rule Explore the informed consent requirements related to increasing understandability and “Key Information." View Webinar Essentials of Grant Proposal Development Take the mystery out of grant writing with in-depth instruction that includes videos, exercises, resources, and examples. View Course Medical Marijuana: A Budding Field of Research Discuss unique challenges and issues as well as considerations for IRB review and steps for getting started in medical marijuana research. View Webinar Bioethics Gain a contemporary understanding about major bioethics concepts, principles, and issues. View Course All Access Webinar Package Access all of CITI Program’s currently available webinar recordings as well as future recordings released during your subscription period. View Package Essentials of Public Health Research Learn about the structure and function of public health systems, differentiate research and practice, and review consent and ethical issues. View Course Clinical Research Coordinator Engage in foundational and advanced role-based training for clinical research professionals. View Courses Communicating Research Findings Focuses on effective practices, guidelines, and strategies for communicating and presenting research findings. View Course Register to take courses developed by experts If you are not affiliated with a subscribing organization, you can register as an independent learner. GET STARTED NOW Subscribe your organization to CITI Program training A base subscription fee includes unlimited access to all core subjects for learners at each of your organization’s sites. Inquire about pricing for additional facilities and large institutions. LEARN MORE CITI Program Subscribers: Protocol Builder Special Offer Sign up for an informational webinar to learn more about Protocol Builder. The online protocol-writing application helps investigators write better quality SBER and NIH protocols and includes training resources for new investigators and residents. Our Special Offer for CITI Program Subscribers: Research Study Design course included with 3-year Protocol Builder subscription. Request A Webinar Content Update News New Webinar: Understanding Consent Requirements and “Key Information” Under the Revised Rule Review new regulatory requirements, learn to develop effective consent materials, and explore "key information" for different types of research. Learn More Blog Webinar - FERPA and Online Learning in the Time of COVID-19 Presented by Thomas Gold, PhD – Acceleration Group, Inc.. This webinar explores how the Family Educational Rights and Privacy Act (FERPA) (20 U.S.C. § 1232g; 34 CFR 99) applies to online learning. The presenter explores student privacy issues and discusses different approaches aimed at safe learning and protecting student information. Review the learning objective and […] Learn More Upcoming Events 5-7 April 2020 - PRIM&R IACUC Conference Attendees will learn about ethical issues and the federal regulations governing animal care and use, best practices for the review and monitoring of research that includes animals, and other timely and late-breaking topics. 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