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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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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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 The program emphasizes new research directions and prohibits the use of unpublished data.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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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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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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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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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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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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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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Multi-Ethnic Study of Atherosclerosis (MESA) recognized outstanding researchers with awards for their contributions to understanding cardiometabolic health, blood pressure control, and cardiovascular disease risk factors among diverse populations. The research findings shed light on the impact of ne

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This content provides a comprehensive guide to Title IX, including its purpose, procedures, training requirements, and the role of investigators and advisors in the complaint process. It covers the definition of Title IX, the purpose of procedures, the hearing process, and the training requirements

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Explore the significance of informed consent in research through examples like the Tuskegee Study, guidance for investigators, and details on who can provide consent. Learn about different types of consent documentation and subject populations that require special approval.

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Explore the significance of adverse event reporting in clinical research, including definitions of adverse events (AEs) and serious adverse events (SAEs), as well as unanticipated problems (UAPs). Learn about the responsibilities of Investigators, Clinical Research Coordinators (CRCs), and Sponsors

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Unravel the intricacies of research set-up focusing on ethics, environment, health, safety, and access to funds discussed during Research Administration Day 2017. Key topics covered include the importance of ethics certifications for all projects, financial control through ethics compliance, and the

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VA ORD investigators are now required to include a Data Management and Access Plan in their proposals effective January 1, 2016. This plan will be evaluated as part of the scientific peer review process. The requirements include provisions for making final research results public, preserving data, e

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This update provides insights into the National Ataxia Foundation's mission to support ataxia research by funding new investigators and treatments. It details funded research in 2015 and 2016, including seed grants, SCA pioneer grants, and grants for young investigators. The focus is on fostering ad

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Dive into the world of research at the upcoming Application and Research Design Workshop scheduled for Friday, 28th May 2021. Discover the strategic priorities driving impactful research initiatives, learn about current research projects, funding processes, and collaborations. Explore the rich histo

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Explore the world of Human Subject Research and Just-In-Time (JIT) process as explained by Assistant Director Cat Sutherland at COMIRB. Learn about exempt categories, secondary research, grant approvals, and the intricate JIT process. Get insights into education research, surveys, behavioral interve

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During the site visit by the Office of Research Oversight (ORO), protocols will be reviewed in depth, including interviews with selected Principal Investigators (PIs) and assessment of training records. ORO will inspect all research areas, identifying areas of noncompliance that will require a Remed

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EDRN investigators can approach the FDA for pre-submission without an industry partner for proposed early detection study designs. The process involves validation, verification, and discovery stages in the biomarker pipeline, utilizing various technologies and biospecimen sets. An example from the o

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Clinical research workflow optimization aims to streamline the process of subject enrollment, study approval, and Epic integration. It involves linking encounters to research studies, using automated tools for transactional data, and enhancing the research workqueue training. The process includes au

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This presentation provides basic information on employment investigations, focusing on the roles and procedures of Title IX Coordinators, Investigators, and Decision Makers. It covers important aspects such as handling formal complaints, mandatory and permissive dismissal criteria, and the philosoph

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