Adaptive tree-based protocol for managing overlay networks in heterogeneous networks. It proposes improvements to the existing Tree-Based Convergecast Routing (TBCR) protocol by considering additional parameters such as RTT, power consumption, link stability, and link mobility to optimize routing de

32 views • 12 slides

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

4 views • 11 slides

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.

1 views • 19 slides

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.

1 views • 17 slides

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

3 views • 34 slides

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

1 views • 12 slides

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.

0 views • 40 slides

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

0 views • 23 slides

Explore the concept of layering in data communication, comparing the OSI model and TCP/IP protocol suite. Learn about protocol layers, protocol hierarchies, and the functionality of each layer in these models. Discover the interrelationships between layers and the evolution from OSI to TCP/IP.

5 views • 57 slides

In 2014, the Memorial Committee of the London Homeless Coalition (LHC) established the Death Communication Protocol to acknowledge, share, and address the loss of individuals experiencing homelessness. The protocol aims to inform partnering organizations of confirmed or unconfirmed deaths, support g

0 views • 12 slides

Mobile computing is crucial for continuous internet connectivity regardless of physical location. The TCP/IP protocol suite, consisting of Transmission Control Protocol (TCP) and Internet Protocol (IP), forms the backbone of internet infrastructure. IP addressing and mobility challenges are addresse

1 views • 51 slides

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

0 views • 16 slides

This chapter explores the OSI model and TCP/IP protocol suite, delving into protocol layers, addressing mechanisms, and network components. It highlights the interface between layers, functions of each layer in the OSI model, and compares TCP/IP protocol suite layers with OSI model layers. The discu

0 views • 30 slides

The MAAP (Multicast Address Acquisition Protocol) is defined in IEEE 1722 for time-sensitive applications in bridged local area networks. It involves acquiring multicast addresses through claiming, probing, and defending messages. MAAP enables dynamic allocation of addresses and defending against co

1 views • 8 slides

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

0 views • 12 slides

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

0 views • 27 slides

This document outlines the ranging protocol proposed for IEEE 802.11-20/1761r1, focusing on RTT-based ranging leveraging multi-channel operation. By integrating the 11az ranging protocol, it enables flexible and low-overhead application in 11bd for improved accuracy in ITS bands. The protocol includ

1 views • 13 slides

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

0 views • 20 slides

Enhanced Interior Gateway Routing Protocol (EIGRP) is a dynamic routing protocol providing various advantages to network administrators. It is a classless routing protocol supporting VLSM and is considered an Interior Gateway Protocol (IGP). EIGRP uses advanced distance vector routing and is known f

1 views • 5 slides

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

0 views • 27 slides

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

4 views • 11 slides

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

1 views • 26 slides

SFTP (SSH File Transfer Protocol) is a secure network protocol for file access, transfer, and management over reliable data streams. It enhances security by extending the SSH protocol and can be implemented using a reliable 8-bit byte stream protocol. SFTP commands are sent as 4 ASCII letters follow

4 views • 23 slides

The 2024 Family Court Police Disclosure Protocol addresses key issues identified in the 2013 protocol, emphasizing timely and proportionate requests for material. Changes include a new checklist for the judiciary, guidance notes, and revised processes for litigants in person. The protocol provides c

1 views • 19 slides

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

0 views • 6 slides

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

0 views • 52 slides

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

0 views • 17 slides

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

0 views • 6 slides

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

0 views • 24 slides

Discover the Saint Leo IRB review process, its purpose, requirements for research approval, definitions of human subjects and research, and how to apply for IRB approval. Learn about the exclusion criteria for class activities and access useful resources and guidance for conducting research at Saint

0 views • 17 slides

This content delves into the roles and responsibilities involved when relying on an external IRB, covering regulatory requirements, the reliance request process, why local context review is essential, and more. It discusses NIH policies, the use of a single IRB for multi-site research, exceptions to

0 views • 40 slides

Delve into the essential aspects of the IRB review process with Dr. Kathryn Greene, a professor and IRB board member. Explore the historical context, regulations, significance, and procedures involved in navigating the IRB review process. Gain insights into the importance of IRB in protecting human

0 views • 27 slides

Protocol deviations are expected occurrences in clinical trials that may arise from site or participant actions. It is crucial for research teams to identify, report, and learn from these deviations to ensure the integrity and safety of the study. Mechanisms for identifying and reporting deviations,

0 views • 16 slides

This detailed content provides an introduction and overview of the Institutional Review Board (IRB), covering its history, purpose, application process, and available resources. The IRB ensures that research involving humans adheres to ethical principles and regulatory requirements to protect partic

0 views • 4 slides

This tutorial guides Investigators (PIs and co-PIs) on how to review IRB reviewer comments in Cayuse after receiving a protocol application feedback. It includes steps on logging into Cayuse, accessing the study details, addressing reviewer comments, and making necessary changes in the protocol. Vis

0 views • 14 slides

This tutorial guides researchers through the process of submitting additional study submissions in Cayuse for tasks such as renewal, modification, incident reporting, or closure, assuming they have an approved IRB protocol. It explains key steps, like logging in, selecting the study, choosing the ty

0 views • 13 slides

This document discusses the proposed Universal Frame Format for a next-generation data link protocol, focusing on major questions about transfer frames, Protocol Link Transmission Unit (PLTU), and Universal Transfer Frame Structure. It explores topics such as frame formats, telemetry transfer frames

0 views • 24 slides

This protocol outlines the benefits and procedure for prone positioning in non-intubated patients experiencing mild to moderate hypoxemia. It highlights patient eligibility criteria, equipment required, and considerations for nursing care. The protocol emphasizes improving oxygenation by promoting a

0 views • 11 slides

Understand the importance of an Institutional Review Board (IRB) for ethical research conduct. Learn about the purpose of an IRB, dispelling myths, roles of faculty advisors and students, and the approval process. Double IRBs may be required in certain cases. Follow the outlined steps for a successf

0 views • 16 slides

New members joining the IRB-03 Research Team at VA facilities must complete specific VA training and administrative tasks before gaining access to data processing equipment. Activities must align with VA appointment types, including Without Compensation, Term/temporary, and Contract Appointments. Th

0 views • 7 slides