Collaborative research opportunity between the U.S. National Science Foundation (NSF) and the Department of Science and Technology (DST) of the Government of India aims to develop new knowledge in computing and communications fields. Investigators from both countries collaborate to write a single pr

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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 BYERS YOUNG INVESTIGATORS RESEARCH CONFERENCE (BYIRC) will be held fully in-person on April 21st, 2023, at Byers Eye Institute in Palo Alto, CA. The event will feature speakers and moderators following specific session formats. Speakers are advised to create presentations tailored to a broad aud

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Explore various early career research funding opportunities such as ONR YIP, AFOSR YIP, ARO YIP, and DARPA YFA programs during the workshop on Friday, May 5, 2023, from 2 to 4 pm at Morris Library 752. These programs offer substantial grants to support young investigators in advancing basic research

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UCC's Research Support, Policy & Strategy function, led by David O'Connell, PhD, provides comprehensive support for research activities at the university. The office manages research funding, monitors performance, and facilitates engagement with external stakeholders. UCC's involvement in Horizon Eu

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This content delves into National Security Presidential Memorandum-33 (NSPM-33) and its implications for individuals associated with research and development projects receiving Federal funding at Indiana University. It explains the requirements, standards, and compliance guidelines set forth by NSPM

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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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Explore the evolution of ethical protections in research involving human subjects, from key historical events to current regulations governing VA research. Understand the responsibilities of investigators and entities in the approval process, along with pathways for accessing drugs via FDA's Expande

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Learn about the fundamentals of research proposals for health-related studies, including defining research, understanding the purposes of health research, and exploring motivation for undertaking research. Discover the difference between basic and applied research, examine types of research, and del

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The Katz ESI R01 Award Program, led by Dr. Stephen I. Katz, offers substantial research project awards for Early Stage Investigators without the need for preliminary data. The program emphasizes new research directions and prohibits the use of unpublished data. Applicants must focus on novel approac

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Understanding the importance of defining a research problem, this content delves into the selection and formulation of research problems, the definition of a research problem, reasons for defining it, methods for identifying research problems, sources of research problems, and considerations in sele

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Research is a systematic pursuit of new knowledge, aiming to unveil hidden truths through data collection and analysis. This course outline delves into the fundamentals of research, covering topics such as types of research studies, importance of research, and distinctions between pure and applied r

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Explore the challenges in conducting research in medical education, emphasizing the importance of evidence-based practices and the need for educators to engage in scholarly activities. Highlighted obstacles include lack of research training, time constraints, and funding issues faced by investigator

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Explore Epic tools for clinical research developed by Shara Power, a skilled application developer specializing in EPIC Beacon Oncology at UIHC Healthcare Information Systems. Learn about managing research study records, investigational study medication orders, and the process for creating and using

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Delve into the world of research paradigms in qualitative medical research with a focus on the key differences between objective and subjective research, the meaning of research paradigms, components of research paradigms, types of research paradigms, and how paradigms guide the selection of researc

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The Research Support Division (RSD) program at the VA focuses on providing guidance and implementing enterprise information security standards for stakeholders involved in research programs. Their mission includes ensuring data security, risk management, and transparency while advancing VA Research.

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Research is crucial for addressing environmental health issues. Choosing a good research topic is the first step towards effective research. This paper discusses the meaning, characteristics, types of research, and the research process to help in selecting appropriate research topics. Understanding

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Key responsibilities of investigators in clinical research involve ensuring participant safety, compliance with regulations, accurate data collection, and ethical conduct throughout the study process. Properly trained investigators play a crucial role in the success and integrity of clinical trials.

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This training addresses the ethical principles and regulations governing VA research involving human subjects, focusing on conducting FDA-regulated Expanded Access Program activities for Monkeypox treatment. It covers historical events shaping research practices, key responsibilities of investigator

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Delve into the Research Training Programme offered by the Graduate School of Social Sciences, led by Professor Mark Tranmer. Explore the importance of research methods training, course offerings under the Research Training Programme (RTP), the Certificate in Social Science Research Methods (CSSRM),

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The UGA Human Research Protection Program (HRPP) aims to ensure the rights and welfare of research subjects by adhering to ethical and regulatory standards. This program consists of various components such as Institutional Leadership, Human Subjects Office, IRBs, Investigators, and more, with a miss

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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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A handbook for RGCB Investigators providing guidelines for submitting research proposals and protocols to the IHEC committee. It includes information on the composition of the EC Regulatory Body, submission procedures, decision processes, and the purpose of EC review to ensure the safety and well-be

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Faculty members can be reassigned or released from their regular duties to work on grants, with a percentage of their time specified for grant-related activities. This process involves communication between the Office of the Comptroller, analysts, principal investigators, and department chairs to ve

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Export control regulations are in place to limit the transfer of certain technology and equipment to specific countries or individuals for national and economic security reasons. Violations can lead to severe sanctions, making it crucial for investigators to be aware of the complex and changing regu

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This content provides guidance on continuing review and renewal processes required for IRB protocols, outlining the importance of ongoing oversight, key submission information, review schedules, and renewal submission procedures. It emphasizes the need for researchers to adhere to regulatory require

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The Icelandic Research Fund (IRF) aims to enhance scientific research and education in Iceland by awarding funding to research projects led by individuals, teams, universities, research institutes, and companies. Principal investigators must have completed graduate studies and experience in running

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PIPERS is a research project focusing on polynyas, ice production, and the seasonal evolution in the Ross Sea. The project involves multiple investigators and coordinated programs to improve estimates of sea ice production, water mass transformation, and air-ice-ocean interactions in the region. Goa

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This document outlines the post-award cycle for December 2021, starting from award notification to sponsor reporting requirements and close-out procedures. It covers the responsibilities of fiscal officers and principal investigators, including account setup, expenditure monitoring, payroll processi

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This presentation discusses the sponsor expectations for clinical studies, investigator responsibilities, TJU's strengths in conducting studies, and how principal investigators can impress sponsors. Topics include assessment of investigator performance, regulatory guidelines, streamlining processes,

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The Fusion Science Department Enabling Research Projects for 2021-2023 focus on developing novel fusion-relevant scientific and technological ideas. These projects, led by Principal Investigators, are distinct from main work packages and involve scientific planning, team collaboration, and resource

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The Collaborative Legal Assistance Program (AIP) is a federally funded collaboration between SADO and MAACS aimed at providing greater access to investigators, training on spotting and litigating extra-record issues, and research and writing support in cases needing expert assistance. The program is

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Explore the functionalities of xTrain in the electronic Research Administration (eRA) Commons by NIH, enabling efficient processing of grant-related activities such as appointments, re-appointments, terminations, and more. Learn about the roles of users, from Program Directors/Principal Investigator

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Safety practices and reporting in clinical research are crucial for ensuring the rights, safety, and well-being of trial subjects. This includes monitoring safety, reporting adverse events promptly, and following regulatory requirements. Investigators play a vital role in assuring subject safety and

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This monthly webinar for VA Innovation and Research Review System (VAIRRS) provides key updates and information for attendees. Topics covered include housekeeping instructions, upcoming events, important announcements such as COVID-19 research dashboard and VAEDA webinar, and a focus on IRBNet basic

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Principal Investigators with a Biological Use Authorization at UC Berkeley must provide lab-specific biosafety training to research group members. This training template covers CLEB administrative requirements, risk assessment, good work practices, emergency procedures, and more. Compliance ensures

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This training template is designed to assist Principal Investigators in providing lab-specific biosafety training to research group members working with recombinant DNA. It covers essential topics such as NIH guidelines, administrative requirements, risk assessment, emergency procedures, and more. C

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Resources and guidance for identifying individuals engaged in human subject's research protocols, including who should be part of the research team, requirements for Principal Investigators, and determining institutional engagement. Learn from the expertise of UMB professionals and access helpful in

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Functional Annotation of Animal Genomes (FAANG) is crucial for associating sequence variation with quantitative phenotypes in domestic animals, serving as important models for human health, disease, and ecology. The NIH actively participates in various genome projects involving cattle, horses, and c

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These guidelines aim to assist research investigators in ensuring the continuity of research operations during emergencies involving drugs and devices. Key actions include obtaining emergency contact numbers, providing emergency cards to participants, securing essential files, communicating with res

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