Pediatric Ethics Subcommittee of the Pediatric Advisory Committee; Notice of Meeting, 30126-30127 [05-10437]

Agencies

• Food and Drug Administration
• DEPARTMENT OF HEALTH AND HUMAN SERVICES

[Federal Register Volume 70, Number 100 (Wednesday, May 25, 2005)]
[Notices]
[Pages 30126-30127]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-10437]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 2005N-0184]


Pediatric Ethics Subcommittee of the Pediatric Advisory 
Committee; Notice of Meeting

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

-----------------------------------------------------------------------

    This notice announces a forthcoming meeting of the Pediatric Ethics 
Subcommittee of the Pediatric Advisory Committee of the Food and Drug 
Administration (FDA). The meeting will be open to the public.
    Name of Committee: Pediatric Ethics Subcommittee of the Pediatric 
Advisory Committee.
    General Function of the Committee: To provide advice and 
recommendations to the Pediatric Advisory Committee on certain 
regulatory issues with regard to FDA and Department of Health and Human 
Services (HHS).
    Date and Time: The meeting will be held on June 28, 2005, from 8:30 
a.m. to 4 p.m.
    Addresses: Electronic copies of the documents for public review can 
be viewed at the Pediatric Advisory Committee (PAC) Docket site at 
https://www.fda.gov/ohrms/dockets/ac/acmenu.htm. (Click on the year 2005 
and scroll down to Pediatric Ethics Subcommittee meeting for 06-28-05.) 
Electronic comments should be submitted to https://www.fda.gov/dockets/
ecomments. Select Docket No. 2005N-0184, entitled ``Surfactant IRB 
Referral'' and follow the prompts to submit your statement. Written 
comments should be submitted to Division of Dockets Management (HFA-

[[Page 30127]]

305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, 
Rockville, MD 20852. Please submit comments by June 7, 2005. Received 
comments may be viewed on the FDA Web site at: https://www.fda.gov/
ohrms/dockets, or may be seen in the Division of Dockets Management 
between 9 a.m. and 4 p.m., Monday through Friday.
    Location: U.S. Food and Drug Administration, 5630 Fishers Lane, rm. 
1066, Rockville, MD.
    Contact Person: Jan N. Johannessen, Office of the Commissioner (HF-
33), Food and Drug Administration, 5600 Fishers Lane (for express 
delivery, rm. 14C-06), Rockville, MD 20857, 301-827-6687, or by e-mail: 
jjohannessen@fda.gov. Please call the FDA Advisory Information Line, 1-
800-741-8138 (301-443-0572 in the Washington, DC area), code 
8732310001, for up-to-date information on this meeting.
    Agenda: The Pediatric Ethics Subcommittee of the Pediatric Advisory 
Committee will meet to discuss a referral by an Institutional Review 
Board (IRB) of a proposed clinical investigation that involves both an 
FDA regulated product and research involving children as subjects that 
may be supported by HHS. The proposed clinical investigation is 
entitled ``Precursor Preference in Surfactant Synthesis of Newborns.'' 
Because the proposed clinical investigation would be regulated by FDA, 
and conducted or supported by HHS; both FDA and the Office for Human 
Research Protections, HHS, will participate in the meeting.
    After presentation of an overview of the IRB referral process, 
background information on surfactant synthesis, an overview of the 
protocol and the referring IRB's deliberations on the protocol, and a 
summary of public comments received concerning whether the protocol 
should proceed, the subcommittee will discuss the proposed protocol and 
develop a recommendation regarding whether the protocol should proceed. 
The subcommittee's recommendation will then be presented to the FDA 
Pediatric Advisory Committee on June 29, 2005; the announcement of the 
June 29 and June 30, 2005, meeting can be found elsewhere in this issue 
of the Federal Register.
    Also elsewhere in this issue of the Federal Register is a notice 
announcing a public comment period concerning whether the proposed 
clinical investigation should proceed. Information regarding submitting 
comments during that period is contained in that notice.
    The background materials for the subcommittee meeting will be made 
publicly available no later than one day before the meeting and will be 
posted under the PAC Docket site at https://www.fda.gov/ohrms/dockets/
ac/acmenu.htm. (Click on the year 2005 and scroll down to Pediatric 
Advisory Committee, Pediatric Ethics Subcommittee meetings.)
    Procedure: Interested persons may present data, information, or 
views, orally or in writing, on issues pending before the subcommittee. 
Written submissions may be made to the contact person by June 17, 2005. 
Oral presentations from the public will be scheduled between 
approximately 11 a.m. and 12 noon.
    Time allotted for each presentation may be limited. Those desiring 
to make formal oral presentations should notify the contact person by 
June 17, 2005, and submit a brief statement of the general nature of 
the evidence or arguments they wish to present, the names and addresses 
of proposed participants, and an indication of the approximate time 
requested to make their presentation.
    Persons attending FDA's advisory committee meetings are advised 
that the agency is not responsible for providing access to electrical 
outlets.
    FDA welcomes the attendance of the public at its advisory committee 
meetings and will make every effort to accommodate persons with 
physical disabilities or special needs. If you require special 
accommodations due to a disability, please notify Jan Johannessen at 
least 7 days prior to the meeting.
    Notice of this meeting is given under the Federal Advisory 
Committee Act (5 U.S.C. app. 2).

    Dated: May 19, 2005.
Sheila Dearybury Walcoff,
Associate Commissioner for External Relations.
[FR Doc. 05-10437 Filed 5-24-05; 8:45 am]
BILLING CODE 4160-01-S