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

3 views • 18 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 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

1 views • 12 slides

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

0 views • 17 slides

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

3 views • 17 slides

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

0 views • 57 slides

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.

0 views • 62 slides

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

0 views • 25 slides

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

0 views • 9 slides

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

0 views • 30 slides

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.

2 views • 16 slides

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.

2 views • 81 slides

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

0 views • 25 slides

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

0 views • 9 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

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

1 views • 20 slides

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

0 views • 11 slides

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

4 views • 12 slides

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

0 views • 19 slides

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

0 views • 22 slides

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

0 views • 6 slides

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

0 views • 6 slides

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,

0 views • 11 slides

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

0 views • 11 slides

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

0 views • 20 slides

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

0 views • 35 slides

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

0 views • 33 slides

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

0 views • 49 slides

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

0 views • 17 slides

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

0 views • 22 slides

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

0 views • 35 slides

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

0 views • 10 slides

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

0 views • 10 slides

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

0 views • 6 slides

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

1 views • 47 slides

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.

0 views • 20 slides

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

0 views • 63 slides

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

0 views • 15 slides

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

0 views • 17 slides

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

0 views • 16 slides