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Second Annual Sentinel Initiative Public Workshop

---
identifier: "/us/fr/E9-30971"
source: "fr"
legal_status: "authoritative_unofficial"
title: "Second Annual Sentinel Initiative Public Workshop"
title_number: 0
title_name: "Federal Register"
section_number: "E9-30971"
section_name: "Second Annual Sentinel Initiative Public Workshop"
positive_law: false
currency: "2009-12-30"
last_updated: "2009-12-30"
format_version: "1.1.0"
generator: "[email protected]"
agency: "Health and Human Services Department"
document_number: "E9-30971"
document_type: "notice"
publication_date: "2009-12-30"
agencies:
  - "Health and Human Services Department"
  - "Food and Drug Administration"
fr_citation: "74 FR 69122"
fr_volume: 74
docket_ids:
  - "Docket No. FDA-2009-N-0664"
fr_action: "Notice of public workshop."
---

#  Second Annual Sentinel Initiative Public Workshop

**AGENCY:**

Food and Drug Administration, HHS.

**ACTION:**

Notice of public workshop.

The Food and Drug Administration (FDA) is announcing the following workshop: Second Annual Sentinel Initiative Public Workshop. This 1-day workshop, organized and hosted by the Engelberg Center for Health Care Reform at Brookings, is supported by a grant from FDA. This workshop is intended to communicate the current status and future vision of active medical product surveillance activities and explore stakeholder perspectives on a broad range of issues. The workshop will feature a series of presentations on recently completed FDA contracts to inform various aspects of the development of the Sentinel System; an update on FDA's ongoing pilot projects in active surveillance of medical product safety; and a discussion of three issues of broad interest: maintaining patient privacy while conducting medical product safety surveillance, developing the Sentinel System as a national resource for medical product safety surveillance for others outside of FDA, and developing a multi-purpose distributed system that can be used to conduct safety surveillance, comparative effectiveness research, product quality assessment and to address other types of public health questions.

*Date and Time:* The workshop will be held on January 11, 2010, from 8:30 a.m. to 4:45 p.m.

*Location:* The workshop will be held at Marriott Metro Center at 775 12th Street NW., Washington, DC 20005.

*Contact:* Kayla Garvin, Center for Drug Evaluation and Research, Bldg. 22, rm. 4339, Food and Drug Administration, 10903 New Hampshire Ave., Silver Spring, MD 20903, 301-796-3755, e-mail: *[email protected].*

*Registration:* To attend the workshop, please register at *http://tinyurl.com/yce6c3z.* When registering, provide the following information: Your name, title, company or organization (if applicable), address, phone number, and e-mail address. There is no fee to register for the public workshop and because seating is limited, registration will be on a first-come, first-served basis. A 1-hour lunch break is scheduled; however no food will be provided. There are multiple restaurants within walking distance of the hotel where attendees can purchase lunch. If you need special accommodations due to a disability, please contact Brookings' event coordinator at 202-797-4391 or by e-mail: *[email protected]* at least 7 days in advance.

*Transcripts:* Please be advised that as soon as a transcript is available, it will be accessible at *http://www.fda.gov/Safety/FDAsSentinelInitiative/ucm149341.htm.* It may be viewed at the Division of Dockets Management (HFA-305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD. A transcript will also be available in either hardcopy or on CD-ROM, after submission of a Freedom of Information request. Written requests are to be sent to the Division of Freedom of Information (HFI-35), Office of Management Programs, Food and Drug Administration, 5600 Fishers Lane, rm. 6-30, Rockville, MD 20857.

Dated: December 23, 2009.

David Horowitz,

Assistant Commissioner for Policy.