Closed meeting June 28, 2018 at National Institutes of Health

Discussion in 'General ME/CFS news' started by MeSci, May 31, 2018.

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  1. MeSci

    MeSci Senior Member (Voting Rights)

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    Location:
    Cornwall, UK
    Source: U.S. Federal Register

    Vol. 83, #105, p 25025

    Date: May 25, 2018

    URL:
    https://www.federalregister.gov/doc...r-scientific-review-notice-of-closed-meetings

    https://www.gpo.gov/fdsys/pkg/FR-2018-05-31/pdf/2018-11722.pdf

    [A Notice by the National Institutes of Health]

    Center for Scientific Review; Notice of Closed Meetings
    -------------------------------------------------------

    Name of Committee: Center for Scientific Review Special Emphasis Panel; Myalgic Encephalomyelitis/Chronic Fatigue Syndrome.

    Date: June 28, 2018.

    Time: 11:00 a.m. to 4:00 p.m.

    Agenda: To review and evaluate grant applications.

    Place: National Institutes of Health, 6701 Rockledge Drive, Bethesda, MD 20892 (Telephone Conference Call).

    Contact Person: Jana Drgonova, Ph.D., Scientific Review Officer, Center for Scientific Review, National Institutes of Health, 6701 Rockledge Drive, Room 5213, Bethesda, MD 20892, 301-827-2549,

    jdrgonova@mail.nih.gov.

    Dated: May 25, 2018.

    Sylvia L. Neal,

    Program Analyst, Office of Federal Advisory Committee Policy.

    [FR Doc. 2018-11722 Filed 5-30-18; 8:45 am]
    BILLING CODE 4140-01-P
     
    Daisymay, Melanie, Skycloud and 10 others like this.
  2. Sunshine3

    Sunshine3 Senior Member (Voting Rights)

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    Fingers crossed Mark Davis and Ron Davis get funding
     
    alktipping, petrichor, BurnA and 4 others like this.
  3. Trish

    Trish Moderator Staff Member

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    UK
    Fingers crossed lots of good bids go in and get funding.
     
  4. Hoopoe

    Hoopoe Senior Member (Voting Rights)

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    What does it mean that such a meeting is held? Is this how grant applications are normally reviewed, or is it special meeting justified by particular circumstances?

    This bit

    suggests there is special emphasis.

    My wild fantasy: they will shove as much money as they can into grants, word will get around that it's easy to get grants for ME/CFS, and we will see more research. Some studies of questionable quality, others of good quality WITH high sample size.
     
    Last edited: May 31, 2018
  5. Sunshine3

    Sunshine3 Senior Member (Voting Rights)

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    Funny how our 'wild fantasies' change with illness....I share your wild fantasy :hug:
     
    alktipping, Daisymay and Hoopoe like this.

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