Drugs

Data and Methods for Evaluating the Impact of Opioid Formulations with Properties Designed to Deter Abuse in the Postmarket Setting: A Scientific Discussion of Present and Future Capabilities

The purpose of the public workshop is to host a scientific discussion with expert panel members and interested stakeholders about the challenges in using the currently available data and methods for assessing the impact of opioid formulations with abuse-deterrent properties on opioid misuse, abuse, addiction, overdose, and death in the postmarket setting. The goal of this meeting is to discuss ways to improve the analysis and interpretation of existing data, as well as to discuss opportunities and challenges for collecting and/or linking additional data to improve national surveillance and research capabilities in this area.

Date:

July 10, 2017 from 8:30 a.m. to 5:00 p.m.
July 11, 2017 from 8:30 a.m. to 5:00 p.m.

Location:

Sheraton Silver Spring
8777 Georgia Avenue
Silver Spring, MD 20910
Tel: 301-589-0800

Registration:

To register to attend the public workshop, Data and Methods for Evaluating the Impact of Opioid Formulations with Properties Designed to Deter Abuse in the Postmarket Setting: A Scientific Discussion of Present and Future Capabilities, in person or virtually via webcast, please register using the link: http://www.cvent.com/d/r5qc6n/4Wdisclaimer icon by June 26, 2017. Please provide complete contact information for each attendee, including name, title, affiliation, address, email, and telephone. If you have any questions with registration, please contact Cherice Holloway at cherice.holloway@fda.hhs.gov.

Streaming Webcast of the Public Workshop:

This public workshop will also be available via web cast for those who have registered by June 26, 2017. Additional information will be made available regarding the accessing of the webcast at least two days prior to the public workshop at: http://www.fda.gov/Drugs/NewsEvents/ucm540845.htm.

Meeting Materials

Transcripts:

Please be advised that as soon as a transcript of the public workshop is available, it will be accessible at https://www.regulations.gov. It may be viewed at the Division of Dockets Management (see ADDRESSES). A link to the transcript will also be available on the Internet at http://www.fda.gov/Drugs/NewsEvents/ucm540845.htm.

Division of Dockets Management (HFA-305)
Food and Drug Administration
5630 Fishers Lane, Rm. 1061
Rockville, MD 20852

Comments on the Public Workshop:

Please refer to the Federal Register Notice on instructions for submitting either electronic or written comments on this public workshop. The deadline for comments is September 11, 2017.

For further information contact:

Scientific Contact:
Cynthia Kornegay
Food and Drug Administration
10903 New Hampshire Avenue
Building 22, Room 2456, Silver Spring, MD, 20993-0002
Tel: 301-796-0187, Email: Cynthia.Kornegay@fda.hhs.gov

Logistics Contact:
Cherice Holloway
Food and Drug Administration
10903 New Hampshire Avenue
Building 22, Room 4466, Silver Spring, MD, 20993-0002
Tel: 301-796-4909, Email: Cherice.Holloway@fda.hhs.gov

 

Page Last Updated: 06/15/2017
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