Learn about the significance of IRB review, levels of review, and categories of expedited review. Discover the criteria for IRB review, including whether the study involves human subjects and contributes to generalizable knowledge. Explore the different levels of IRB review and the specific categori

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The basics of the IRB, researcher responsibilities, IRB members, and the role of faculty advisors and student investigators in navigating the IRB application process. Understand the importance of ancillary approvals for research projects involving human subjects.

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The content provides an overview of the IRB review process for research studies, including what necessitates IRB review, the levels of IRB review (exempt, expedited, full board), examples of full board research, and criteria for an Investigational New Drug.

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Increase in cybersecurity threats necessitates the use of two-factor authentication in the Funding & Tenders Portal to safeguard valuable information. Users are encouraged to adopt this secure login method, which will soon become mandatory. Methods such as mobile devices, SMS, and security keys are

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Delve into the world of research ethics through an overview of Institutional Review Boards (IRB), regulations governing human subjects research, historical events shaping research ethics, and examples of research controversies. Explore key ethical principles and the role of the IRB in protecting res

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Explore key aspects of VA Central IRB approval, continuing review for multi-site projects, process structure, changes in documentation, and future updates. Learn about criteria for approval, VHA policy compliance, informed consent requirements, and more.

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Reviewing IRB applications involves checking for completion of necessary information, ensuring proper student researcher listing with faculty sponsor, verifying logical data collection dates and participant numbers, reviewing research design, assessing instruments used, examining recruitment and sel

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Explore the levels of IRB review for human participant research, including Exempt, Expedited, and Full Board reviews. Learn about the categories of Exempt Determinations and the criteria for Limited IRB Review. Understand if your study requires IRB review based on research and human subject involvem

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Providing essential guidance for first-time researchers submitting to the Barry University IRB in January 2023. Covers initial steps such as creating an IRBNet account, completing ethics training, determining the review category, and selecting the appropriate protocol form.

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Human Subject Research Protections at Villanova IRB, including regulatory background, review process, and key information for investigators. Learn about the Institutional Review Board structure, ethical principles, and historical background of human subjects research at Villanova University.

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IRB reliance agreements allow institutions to delegate IRB review responsibilities or collaborate with other institutions for human subjects research. Federalwide assurance (FWA) documents ensure compliance with regulations. Different types of agreements, such as IRB authorization agreements and ind

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Learn how to create your EU Login account and add two-factor authentication for accessing Europass and other EU services. Follow step-by-step instructions to register, verify your email, and set up a secure password. Ensure a seamless process by understanding the difference between Europass and EU L

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Exploring different types of research and IRB applications in academic studies, including processes related to contact registries, data/tissue banks, and consent management. The content provides insights into engaging specific populations for future research, collecting and storing clinical data, ut

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Learn about the implementation of two-step authentication at a university to combat phishing attacks and enhance security. Discover how Duo Security was used to provide a seamless two-step authentication solution, the challenges faced during the enrollment tool setup, and the successful implementati

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Pathology Department's IRB protocol enables the screening of electronic medical records for research purposes, allowing members to review patient records and pathology slides. By fulfilling specific requirements and obtaining blanket IRB approval, researchers can access and analyze patient data for

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Research Compliance Administrator, Sharla Miles, M.Ed., CIP, provides guidance on using Cayuse IRB for creating and completing initial study submissions. Learn to navigate the system, enter study details, and submit for review efficiently.

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The GPS IRB at Pepperdine University focuses on protecting the rights and welfare of human research subjects. Applications cover social, behavioral, and educational research, following federal regulations. IRB approval is required before starting any research activities, and different application ty

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Explore the implementation of two-factor authentication (2FA) for UW Azure Active Directory (AD) based on key decisions and options outlined in the provided slides. Understand the strategies for enforcing MFA, handling legacy authentication, and transitioning to cloud-based authentication. Discover

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Explore the subcommittee report on security and authentication in electronic filing systems for campaign and finance reports in Arkansas. Learn about user authentication, risks, mitigation strategies, and approaches used in other states. Discover the filing processes in both paper and electronic for

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This comprehensive overview delves into the IRB application process, covering topics such as human research protections, IRB oversight requirements, different types of reviews, informed consent, response to IRB correspondence, common errors, and the significance of ethics in research. Key historical

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Institutional Review Board (IRB) plays a crucial role in ensuring research involving human subjects adheres to ethical standards. This summary provides insights into the IRB process, including determining the need for IRB review, defining human subjects research, and the importance of human subjects

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Learn about key regulatory requirements and best practices for convening and conducting an Institutional Review Board (IRB) meeting. This guide covers pre-meeting activities, achieving quorum, member attendance, conflicts of interest, and more.

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Institutional Review Board (IRB) plays a crucial role in protecting the rights and welfare of research participants, ensuring the validity, ethics, and compliance of human research. This content covers the functions of IRB as a Privacy Board, distinguishes Downstate and non-Downstate workforce inves

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Enhance your understanding of the IRB application process with helpful resources, step-by-step instructions, and access to training modules. From CITI certification to Cayuse navigation, this comprehensive guide aims to simplify the protocol submission journey for researchers. Explore hints, example

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Understanding the IRB process is crucial for conducting ethical research involving human subjects. This guide outlines federal regulations, protective mechanisms, IRB goals, and the definition of human subjects in research. It also provides insights into the level of intervention, considerations whe

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Update on the significant changes in the Revised Common Rule and Proposed VHA Directive 1200.05, focusing on the impact on the IRB, membership, functions, and review of research. Details provided on the status of the Revised Common Rule, VHA Handbook 1200.05, and applicability of pre-2018 and 2018 r

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This resource provides detailed guidance on the requirements and processes for consulting with the Human Subjects Division (HSD) for single Institutional Review Board (IRB) studies involving multiple institutions, federally-funded research, and new NIH funding. It includes information on when a sIRB

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Comprehensive instructions for submitting continuing review information when utilizing an external Institutional Review Board (IRB), including steps such as completing questions, selecting study status, updating funding, adding personnel, and uploading necessary documents.

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The DAVA Drugs Authentication & Verification Application, developed by the National Informatics Centre of the Government of India, enables authentication, tracking, and tracing of Indian drugs at different packaging levels. Manufacturers maintain Unique Serial Numbers for primary and secondary packa

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Learn how to enhance HR system security by setting up two-factor authentication for off-campus access. This tutorial covers the importance of two-factor authentication, using your phone as a second layer of security, initial setup procedures through Wyoweb, requesting permission for HR self-service

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Maria Drayton, an IRB Analyst at the University of Maryland, presents important information on Not Humans Subjects Research (NHSR). This includes definitions, IRB review requirements, evaluation criteria, and actions to take based on research determinations. The process involves careful consideratio

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Explore the essential criteria for human subjects research, the process of applying to the IRB for determinations, understanding regulated research, and common errors in exemption submissions. Delve into expedited vs. full board reviews and different categories of research review, in this detailed g

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This tutorial is for researchers (PIs) with an approved IRB protocol who want to make changes to their study titles and submit renewals, modifications, incidents (adverse events), or closures. Learn about the process in Cayuse, from initial study to amending/modifying, renewing, or closing protocols

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Explore the potential VHA policy changes that can streamline IRB and R&D committee responsibilities to better serve veterans while upholding the VA's mission. Delve into questions concerning beneficial and challenging policy changes, the need for a single R&D committee model, and considerations on t

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Explore the options for setting up Multi-Factor Authentication (MFA) at Moraine Park, with Microsoft Authenticator as the recommended method. You can choose between using the Microsoft Authenticator app on a smartphone, receiving a text message, or a phone call for authentication. Detailed steps for

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Authentication lies at the core of application security, serving as the primary defense against malicious attacks. This article explores various authentication technologies, including HTML forms-based authentication, multi-factor mechanisms, client SSL certificates, and more. It delves into common d

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This article introduces an open-source SPDM (Secure Protocol and Data Model) implementation for secure device communication, developed by Jiewen Yao and Xiaoyu Ruan, Principal Engineers at Intel. SPDM aims to enhance device security through protocols for device authentication, session key establishm

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Explore the world of authentication and authorization in the field of astronomy through the lens of the ASTERICS project. Learn about the importance of verifying identities and granting access rights, the Virtual Observatory Approach, Single Sign-On standards, and Credential Delegation protocols. Di

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The article explores the obsolescence of IP filtering in user authentication, highlighting the challenges posed by evolving technology and the limitations of IP-based authentication methods. It discusses the shift towards improving user experience and addressing security concerns by focusing on user

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This tutorial provides step-by-step instructions for submitting a new IRB protocol in Cayuse IRB. It covers essential preparatory steps, authentication requirements, logging in to Cayuse, navigating the platform, and initiating a new study application. Helpful tips are included for Primary Investiga

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