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Topic: Office of Research Integrity


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In the News (Fri 1 Jan 10)

  
  Guidelines for Ethical Practices
Research subjects already participating in a protocol by virtue of signing an approved consent document must be informed of any new information regarding risks and benefits of study participation when such data become available as the study progresses.
Office of Research (412-624-7400) is the only gateway for submitting and processing research proposals and budgets to sponsoring agencies, whether governmental or private.
Research Conduct and Compliance Office (412-578-3421) oversees and facilitates the conduct of ethical and regulation-compliant human and animal subject research.
www.pitt.edu /~provost/ethresearch.html   (6129 words)

  
 Online Ethics Center: ORI Model Policy for Responding to Allegations of Scientific Misconduct   (Site not responding. Last check: 2007-11-06)
The Research Integrity Officer will be an institutional official who is well qualified to handle the procedural requirements involved and is sensitive to the varied demands made on those who conduct research, those who are accused of misconduct, and those who report apparent misconduct in good faith.
The Research Integrity Officer will provide the respondent with a copy of the draft inquiry report for comment and rebuttal and will provide the whistleblower, if he or she is identifiable, with portions of the draft inquiry report that address the whistleblower's role and opinions in the investigation.
Depending on the particular circumstances, the Research Integrity Officer should consider notifying those individuals aware of or involved in the investigation of the final outcome, publicizing the final outcome in forums in which the allegation of scientific misconduct was previously publicized, or expunging all reference to the scientific misconduct allegation from the respondent's personnel file.
onlineethics.org /colloq/mod.html   (5210 words)

  
 Office of Research Integrity
Where research involves the collection of highly sensitive information about individually identifiable subjects, the IRB may determine that special protections are needed to protect subjects from the risks of investigative or judicial processes.
Every research project that includes human research subjects should explain how identifiable information would be used or disclosed, regardless of whether or not a Certificate is in effect.
The Office of Research Integrity (ORI) personnel are bound by all legal and ethical requirements to protect the rights of human subjects, including the confidentiality of information that can be identified with a person.
www.marshall.edu /research/ori/Sops/PrivacyandConfidentiality.htm   (1353 words)

  
 NIH Guide: RESEARCH ON RESEARCH INTEGRITY
However, information is still lacking on the impact of specific research behaviors and of efforts to promote integrity in research on the research record and the overall practice of research.
This RFA seeks applications for empirical research that adds to understandings of the ways in which research integrity and efforts to promote responsible conduct in research directly or indirectly impact the research record, research institutions, and/or the benefits derived from biomedical and behavioral research.
Relevant research perspectives and disciplines include, but are not limited to: anthropology, applied philosophy, business, economics, education, information studies, law, organizational studies, health services, political science, psychology, sociology, and survey and evaluation research, plus the physical, biomedical, and clinical sciences, including nursing.
grants1.nih.gov /grants/guide/rfa-files/RFA-NS-04-001.html   (2930 words)

  
 Office of Research Integrity
The Office of Research Integrity (ORI) promotes integrity in biomedical and behavioral research supported by the U. Public Health Service (PHS) at about 4,000 institutions worldwide.
ORI monitors institutional investigations of research misconduct and facilitates the responsible conduct of research through educational, preventive, and regulatory activities.
Organizationally, ORI is located in the Office of Public Health and Science (OPHS), within the Office of the Secretary of Health and Human Services (OS), in the U.S. Department of Health and Human Services (HHS).
ori.dhhs.gov   (397 words)

  
 ORI 050623
The UAF Office of Research Integrity (ORI) monitors institutional investigations of research misconduct and facilitates the responsible conduct of research through educational, preventive, and service activities.
Research compliance is coordinated through the activities of the five UAF Research Committees.
Ensuring the integrity of the research record is a continual process involving everyone.
www.uaf.edu /ori   (145 words)

  
 Ethical Issues in Research Involving Human Participants (CBM 99-3)
They are designed to: support research to examine ethical issues surrounding research involving human participants; 8 provide training opportunities in the form of mentored scientist awards in research ethics; 9 and develop short term courses in research ethics.
Although regulatory safeguards for protecting research participants have improved significantly in recent years, 11 historical cases such as the Tuskegee Syphilis Study stand as examples of the potential for ethical problems in research involving human participants, and of the need for vigilance in protecting the rights and welfare of these individuals.
Next, the bibliography focuses on selected populations that may be recruited for research, including: women; minorities; children; the elderly; the cognitively impaired (including those who have mental disorders and whose capacity to consent may be diminished or questionable); prisoners; military personnel; newly deceased individuals; and researchers involved in self-experimentation.
www.nlm.nih.gov /pubs/cbm/hum_exp.html   (10399 words)

  
 Guidelines for the Conduct of Research at NIH   (Site not responding. Last check: 2007-11-06)
Research training is a complex process, the central aspect of which is an extended period of research carried out under the supervision of an experienced scientist.
Research data, including detailed experimental protocols, all primary data, and procedures of reduction and analysis are the essential components of scientific progress.
Research data, including the primary experimental results, should be retained for a sufficient period to allow analysis and repetition by others of published material resulting from those data.
www.nih.gov /campus/irnews/guidelines.htm   (2936 words)

  
 Office of Research Integrity   (Site not responding. Last check: 2007-11-06)
The purpose of the proposed grant program is to foster empirical research on societal, organizational, group, and individual factors that affect, both positively and negatively, integrity in research.
For the purposes of this request for applications (RFA), "research" is interpreted broadly to include societal, organizational, group, and individual aspects of the enterprise.
"Integrity" is understood as "the use of honest and verifiable methods in proposing, performing, and evaluating research in reporting research results with particular attention to adherence to rules, regulations, guidelines, and commonly accepted professional codes or norms." SPECIAL CONSIDERATIONS: ELIGIBILITY CRITERIA: Applications may be submitted by foreign universities.
www.biu.ac.il /RA/www/rserch/calls/calls/ori_integrity.html   (182 words)

  
 OFFICE OF RESEARCH INTEGRITY   (Site not responding. Last check: 2007-11-06)
FFICE OF The Office of Research Integrity is available to faculty, staff, and students to answer questions about the application or interpretation of research integrity standards.
The Office of Research Integrity is responsible for coordinating and overseeing the conduct of inquiries and investigations by peer faculty groups into allegations of research misconduct and for maintaining liaison on these matters with outside agencies that sponsor research.
To consult with the Research Integrity Officer or to request copies of the Research Integrity Policy (University Policy 11-01-01) or the Guidelines for Ethical Practice in Research, telephone 412-624-3007.
www.pitt.edu /~provost/ch4_off_res_int.htm   (119 words)

  
 Human Subjects Research and IRBs - Bioethics Resources on the Web - NIH   (Site not responding. Last check: 2007-11-06)
Research Involving Individuals with Questionable Capacity to Consent: Points to Consider - a report by the Office of Extramural Research.
Scientists and Subjects: A Web-based Seminar on the Ethics of Research with Human Subjects - The Poynter Center for the Study of Ethics and American Institutions, Indiana University.
DOE Office of Human Radiation Experiments - established in March 1994, leads the Department of Energy's efforts to tell the agency's Cold War story of radiation research using human subjects.
www.nih.gov /sigs/bioethics/IRB.html   (1040 words)

  
 Letter to Office of Research Integrity   (Site not responding. Last check: 2007-11-06)
We write in regard to the U.S. Food and Drug Administration's proposed research ban on James M. Wilson at the University of Pennsylvania.
Wilson's judgement and behavior is being considered adequate to ban his experimental use of humans yet no mention is being made of his experiments on animals.
Both academic integrity and public trust demand that decisions regarding Wilson's access to living experimental subjects, whether human or others, be just and equitable.
www.vivisectioninfo.org /news/jwltr.html   (268 words)

  
 Responsible Conduct of Research Conference - Office of Research - Idaho State University   (Site not responding. Last check: 2007-11-06)
The purpose of the conference is to educate the academic community in the areas of Responsible Conduct of Research (RCR), Research Integrity, and Research Misconduct; and to emphasize the importance of mainstreaming this education - making it an integral, and ongoing part of a research or administrative career.
This conference will launch, the first of several Idaho State University Research Office initiatives directed to the research community and students to inform and educate them regarding responsible conduct and research professionalism.
Additionally, this conference is expected to result in an increased understanding among participants of the importance of institutionalizing and engaging in life-long learning in RCR education and skills development.
www.isu.edu /research/rcr   (239 words)

  
 Office of Research Integrity
Conflicts of interest may arise because of the intellectual property involved in many research discoveries or industry-academic partnerships, from financial incentives pharmaceutical or biotech companies may offer researchers or physicians for conducting trials or enrolling subjects, or due to particular role relationships.
Where the IRB Chairperson or member competes for research grants or contracts in the same or similar field as an investigator whose research is scheduled for review.
Financial interests which are subject to reporting for any given research proposal include those which would reasonably appear to be affected by the specific research proposed; and/or are interests in entities whose financial interests would reasonably appear to be affected by the research.
www.marshall.edu /research/ori/Sops/ConflictofInterest.htm   (1296 words)

  
 the videos
Integrity and Misconduct in Research (Washington, DC: Office of Research Integrity, November 1995).
Analysis of Guidelines for the Conduct of Research Adopted by Medical Schools or their Components (Washington, DC: Office of Research Integrity, September 2001); http://ori.dhhs.gov/html/publications/analysisofguidelinesfortheconduct.asp.
Study of the Incidence of Misconduct Report by Institutions (Rockville, MD: Office of Research Integrity); http://ori.dhhs.gov/html/publications/studyoftheincidence.asp.
www.aaas.org /spp/video/reports.htm   (666 words)

  
 IRB Office for Research Integrity at Children's Mercy Hospitals and Clinics
IRB Office for Research Integrity at Children's Mercy Hospitals and Clinics
CMH has a Federalwide Assurance (FWA) with the Department of Health and Human Services, in which we assure Federal officials that any research project, whether it is chart review or administration of investigational drugs, is conducted in accordance with Federal regulations.
Our Office for Research Integrity is here to help you navigate through the process.
www.childrens-mercy.org /irb   (199 words)

  
 NIH Guide: REQUIRED EDUCATION IN THE PROTECTION OF HUMAN RESEARCH PARTICIPANTS
Background To bolster the Federal commitment to the protection of human research participants, several new initiatives to strengthen government oversight of medical research were announced by HHS Secretary Shalala on May 30, 2000.
Related Training Requirement The Office of Research Integrity (ORI), Department of Health and Human Services, is developing a policy to implement an extension of the training requirement on the responsible conduct of research (RCR) to all persons supported by PHS research.
For example, all NIH intramural investigators and research administrators who oversee clinical projects are required to complete an on-line tutorial on the protection of human research subjects.
grants.nih.gov /grants/guide/notice-files/NOT-OD-00-039.html   (705 words)

  
 Office of Research Support Services   (Site not responding. Last check: 2007-11-06)
The Office of Research Integrity and Compliance is charged with and committed to the education of faculty and staff in research regulatory requirements.
The Office of Regulatory Affairs: Fostering a culture of compliance.
Working with researchers, ethicists, and members of the public to assure that all research conducted under the auspices of the University of Pennsylvania honors Penn's standards for the treatment of people and animals.
www.med.upenn.edu /orss/internal_links.shtml   (782 words)

  
 CJ Fearnley's Home Page
Integrity is the most continually important issue in human affairs.
Integrity implies truth: being true to the facts of experience and true to oneself and true to Humanity and true to Earth and true to
Integrity requires consideration and re-consideration of the whole and all of the parts and their
www.cjfearnley.com   (3704 words)

  
 Home Page
NIH is providing information and guidance regarding the HIPAA Privacy Rule and its impact upon research.
An NIH website has been developed to provide the research community with information and resources.
A booklet, entitled Protecting Personal Health Information in Research: Understanding the HIPAA Privacy Rule, is now available (see website for details).
rehabnetwest.washington.edu   (290 words)

  
 Office of Research Integrity   (Site not responding. Last check: 2007-11-06)
The University of Colorado at Boulder is committed to scientific and ethical integrity as well as academic excellence in all research activities with which our students, faculty and staff are associated.
The Office of Research Integrity's role is to assist researchers in conducting research that meets the highest standards of ethical and regulatory compliance and to coordinate the activities of various faculty oversight committees:
The Office of Research Integrity has a representative on the Radiation Safety Committee, and oversees the
www.colorado.edu /GraduateSchool/ORI   (112 words)

  
 Office of Research Administration and Advancement
Office of Research Integrity - Dept of Health and Human Services:
Office of Human Research Protections – Dept of Health and Human Services:
Responsible Conduct of Research: Dr. Lawrence J. Rhoades, Director, ORI and Dr. Nancy Davidian, ORI
www.umresearch.umd.edu /ORAA/workshops/PrelimResDayOL.html   (579 words)

  
 Find in a Library: Office of Research Integrity : an introduction.
Find in a Library: Office of Research Integrity : an introduction.
Medicine -- Research -- Moral and ethical aspects -- United States.
Medical research personnel -- Professional ethics -- United States.
worldcatlibraries.org /wcpa/ow/5865913379042605a19afeb4da09e526.html   (60 words)

  
 CDC - OCSO - Human Research Protection Office - Home Page   (Site not responding. Last check: 2007-11-06)
All research involving human participants conducted by the Centers for Disease Control and Prevention (CDC) or funded in whole or in part by CDC must comply with the Code of Federal Regulations, Title 45, Part 46-Protection of Human Subjects (45 CFR 46).
This includes research conducted by CDC employees, either directly, through, cooperative agreements, contracts or simplified acquisition (e.g., purchase orders) or in collaboration with outside parties.
Additionally, all research must be approved by an Institutional Review Board (IRB) prior to the start of the research.
www.cdc.gov /od/ads/hsr2.htm   (131 words)

  
 term papers - thousands of papers to help with term papers - 1millionpapers.com
*Our research papers are created to be used as models to assist you in the preparation of your own term paper.
Neither 1MillionPapers.Com nor any website owned by The Paper Store Enterprises Inc., will EVER sell a research paper to ANY student giving us ANY reason to believe that (s)he will submit our work, either in whole or part, for academic credit at any institution in their own name.
The organization's rights to research, write, and globally-publish exemplary papers on the Internet are protected, Free Speech and shall continue unabated and uncensored.
www.1millionpapers.com   (329 words)

  
 Administration/Staff : Office for Research : Northwestern University   (Site not responding. Last check: 2007-11-06)
Office for Research Organizational Chart - September 2005 (.pdf format)
Office of Research Analysis and Communication (ORAC)
Mailing address: Vice President for Research, Northwestern University, 633 Clark Street, Evanston, IL 60208-1108
www.northwestern.edu /research/admin-staff   (83 words)

  
 CIRCARE: Office for Human Research Protections – Information
The International Compilation of Human Subject Research Protections, a listing of the laws, regulations, and guidelines that govern human subjects research in many countries around the world.
Office of Research Integrity Case Summaries (Summaries of administrative actions when findings of misconduct are made.)
Office for Civil Rights HIPAA and Privacy of Health Records (US Department of Health and Human Services)
www.circare.org /info5a.htm   (731 words)

  
 RCREC
research community in identifying, developing, and promoting programs
of education in the responsible conduct of research.
Service mark (SM) 2005 Responsible Conduct of Research Education Consortium.
rcrec.org   (82 words)

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