Findings of Research Misconduct, 33137 [2017-15159]

Download as PDF asabaliauskas on DSKBBXCHB2PROD with NOTICES Federal Register / Vol. 82, No. 137 / Wednesday, July 19, 2017 / Notices The meeting agenda will include: (1) Presentations and discussion on the processes states use to identify and follow up on out of range newborn screening results; (2) a presentation on phase one of the spinal muscular atrophy evidence review; (3) presentations on newborn screening topics such as the clinical and public health impact of Critical Congenital Heart Defects, quality measures in newborn screening, and a review of newborn screening technology; and (4) updates from the Laboratory Standards and Procedures workgroup, Follow-up and Treatment workgroup, and Education and Training workgroup. The Committee will not be voting on a proposed addition of a condition to the RUSP. Agenda items are subject to change. The final meeting agenda will be available 2 days prior to the meeting on the Committee’s Web site: https:// www.hrsa.gov/advisorycommittees/ mchbadvisory/heritabledisorders. Members of the public will have the opportunity to provide comments. All comments are part of the official Committee record. To submit written comments or request time for an oral comment at the meeting, please register online by 12:00 p.m. on July 28, 2017, at https://www.achdncmeetings.org/. To ensure all individuals who have registered and requested time for oral comments are accommodated, the allocated time for comments may be limited. Individuals associated with groups or who plan to provide comments on similar topics may be asked to combine their comments and present them through a single representative. No audiovisual presentations are permitted. Written comments should identify the individual’s name, address, email, telephone number, professional or organization affiliation, background or area of expertise (i.e., parent, family member, researcher, clinician, public health) and the topic/subject matter. Individuals who plan to attend and need special assistance, such as sign language interpretation or other reasonable accommodations, should notify Ann Ferrero using the address and phone number above at least 10 days prior to the meeting. Jason E. Bennett, Director, Division of the Executive Secretariat. [FR Doc. 2017–15113 Filed 7–18–17; 8:45 am] BILLING CODE 4165–15–P VerDate Sep<11>2014 18:49 Jul 18, 2017 Jkt 241001 DEPARTMENT OF HEALTH AND HUMAN SERVICES Office of the Secretary Findings of Research Misconduct Office of the Secretary, HHS Notice. AGENCY: ACTION: Notice is hereby given that the Office of Research Integrity (ORI) has taken final action in the following case: Alec Mirchandani, Florida Atlantic University: Based on the report of the inquiry conducted by Florida Atlantic University (FAU), the Respondent’s admission, and analysis conducted by ORI, ORI found that Mr. Alec Mirchandani, former post-baccalaureate research volunteer in the Center for Complex Systems and Brain Sciences, Florida Atlantic University (FAU), engaged in research misconduct in research supported by National Institute of Mental Health (NIMH), National Institutes of Health (NIH), grant 1 R15 MH099590–01A1. ORI found that Respondent engaged in research misconduct by knowingly and intentionally: (1) Fabricating the results of the T-maze behavioral experiment for control mice, (2) falsifying the laboratory and vivarium entry logs in an effort to cover up his actions, and (3) reporting the fabricated and falsified data to his laboratory supervisors. Specifically, ORI found that Respondent knowingly and intentionally: • Fabricated the results that he recorded for the T-maze behavioral experiment in three of the five TMZ control mice on the laboratory data sheets and white board on fourteen (14) of the sixteen (16) eligible days in June 2016, to make it appear as though he had conducted the experiments; • Falsified the animal transfer logs on twelve (12) of the sixteen (16) eligible days in June 2016, to make it appear as though he had conducted the experiments; • Fabricated the times he recorded on the laboratory data sheets on fourteen (14) of the sixteen (16) eligible days in June 2016, to make it appear as though he had conducted the experiments; • incorporated and recorded the fabricated and falsified data with his previous data in his laboratory notebook and reported the results to his laboratory supervisor and principal investigator, such that the experimental control data (five animals) for experiments conducted from January 2016–June 30, 2016, were not accurately represented. SUMMARY: PO 00000 Frm 00098 Fmt 4703 Sfmt 4703 33137 Mr. Mirchandani has entered into a Voluntary Settlement Agreement with ORI, in which he voluntarily agreed, beginning on June 29, 2017: (1) That if within two (2) years from the effective date of the Agreement, Respondent receives or applies for U.S. Public Health Service (PHS) support, Respondent agrees to have his research supervised for a period of one (1) year, beginning on the date of his employment in a position in which he receives or applies for PHS support, and agrees to notify his employer(s)/ institution(s) of the terms of this supervision. Respondent agrees that prior to the submission of an application for PHS support for a research project on which the Respondent’s participation is proposed and prior to Respondent’s participation in any capacity on PHS-supported research, Respondent shall ensure that a plan for supervision of Respondent’s duties is submitted to ORI for approval. The supervision plan must be designed to ensure the scientific integrity of Respondent’s research contribution. Respondent agrees that he shall not participate in any PHS-supported research until such a supervision plan is submitted to and approved by ORI. Respondent agrees to maintain responsibility for compliance with the agreed upon supervision plan. (2) To exclude himself voluntarily from serving in any advisory capacity to PHS including, but not limited to, service on any PHS advisory committee, board, and/or peer review committee, or as a consultant for a period of one (1) year, beginning with the effective date of the Agreement. FOR FURTHER INFORMATION CONTACT: Director, Office of Research Integrity, 1101 Wootton Parkway, Suite 750, Rockville, MD 20852, (240) 453–8200. Kathryn M. Partin, Director, Office of Research Integrity. [FR Doc. 2017–15159 Filed 7–18–17; 8:45 am] BILLING CODE 4150–31–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Institute of Allergy and Infectious Diseases; Notice of Closed Meeting Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended (5 U.S.C. App.), notice is hereby given of the following meeting. The meeting will be closed to the public in accordance with the provisions set forth in sections E:\FR\FM\19JYN1.SGM 19JYN1

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[Federal Register Volume 82, Number 137 (Wednesday, July 19, 2017)]
[Notices]
[Page 33137]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-15159]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Office of the Secretary


Findings of Research Misconduct

AGENCY: Office of the Secretary, HHS

ACTION: Notice.

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SUMMARY: Notice is hereby given that the Office of Research Integrity 
(ORI) has taken final action in the following case:
    Alec Mirchandani, Florida Atlantic University: Based on the report 
of the inquiry conducted by Florida Atlantic University (FAU), the 
Respondent's admission, and analysis conducted by ORI, ORI found that 
Mr. Alec Mirchandani, former post-baccalaureate research volunteer in 
the Center for Complex Systems and Brain Sciences, Florida Atlantic 
University (FAU), engaged in research misconduct in research supported 
by National Institute of Mental Health (NIMH), National Institutes of 
Health (NIH), grant 1 R15 MH099590-01A1.
    ORI found that Respondent engaged in research misconduct by 
knowingly and intentionally: (1) Fabricating the results of the T-maze 
behavioral experiment for control mice, (2) falsifying the laboratory 
and vivarium entry logs in an effort to cover up his actions, and (3) 
reporting the fabricated and falsified data to his laboratory 
supervisors.
    Specifically, ORI found that Respondent knowingly and 
intentionally:
     Fabricated the results that he recorded for the T-maze 
behavioral experiment in three of the five TMZ control mice on the 
laboratory data sheets and white board on fourteen (14) of the sixteen 
(16) eligible days in June 2016, to make it appear as though he had 
conducted the experiments;
     Falsified the animal transfer logs on twelve (12) of the 
sixteen (16) eligible days in June 2016, to make it appear as though he 
had conducted the experiments;
     Fabricated the times he recorded on the laboratory data 
sheets on fourteen (14) of the sixteen (16) eligible days in June 2016, 
to make it appear as though he had conducted the experiments;
     incorporated and recorded the fabricated and falsified 
data with his previous data in his laboratory notebook and reported the 
results to his laboratory supervisor and principal investigator, such 
that the experimental control data (five animals) for experiments 
conducted from January 2016-June 30, 2016, were not accurately 
represented.
    Mr. Mirchandani has entered into a Voluntary Settlement Agreement 
with ORI, in which he voluntarily agreed, beginning on June 29, 2017:
    (1) That if within two (2) years from the effective date of the 
Agreement, Respondent receives or applies for U.S. Public Health 
Service (PHS) support, Respondent agrees to have his research 
supervised for a period of one (1) year, beginning on the date of his 
employment in a position in which he receives or applies for PHS 
support, and agrees to notify his employer(s)/institution(s) of the 
terms of this supervision. Respondent agrees that prior to the 
submission of an application for PHS support for a research project on 
which the Respondent's participation is proposed and prior to 
Respondent's participation in any capacity on PHS-supported research, 
Respondent shall ensure that a plan for supervision of Respondent's 
duties is submitted to ORI for approval. The supervision plan must be 
designed to ensure the scientific integrity of Respondent's research 
contribution. Respondent agrees that he shall not participate in any 
PHS-supported research until such a supervision plan is submitted to 
and approved by ORI. Respondent agrees to maintain responsibility for 
compliance with the agreed upon supervision plan.
    (2) To exclude himself voluntarily from serving in any advisory 
capacity to PHS including, but not limited to, service on any PHS 
advisory committee, board, and/or peer review committee, or as a 
consultant for a period of one (1) year, beginning with the effective 
date of the Agreement.

FOR FURTHER INFORMATION CONTACT: Director, Office of Research 
Integrity, 1101 Wootton Parkway, Suite 750, Rockville, MD 20852, (240) 
453-8200.

Kathryn M. Partin,
Director, Office of Research Integrity.
[FR Doc. 2017-15159 Filed 7-18-17; 8:45 am]
 BILLING CODE 4150-31-P
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