2017-06699. Food and Drug Administration/Xavier University Medical Device Conference (MedCon)  

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    AGENCY:

    Food and Drug Administration, HHS.

    ACTION:

    Notice of public conference.

    SUMMARY:

    The Food and Drug Administration (FDA) Cincinnati District, in co-sponsorship with Xavier University, is announcing a public conference entitled “FDA/Xavier University Medical Device Conference (MedCon).” This 3-day public conference includes presentations from key FDA officials and industry experts with small group break-out sessions. The conference is intended for companies of all sizes and employees at all levels.

    DATES:

    The public conference will be held on May 3, 2017, from 8:30 a.m. to 5 p.m.; May 4, 2017, from 8:30 a.m. to 5 p.m.; and May 5, 2017, from 8:30 a.m. to 12:30 p.m.

    ADDRESSES:

    The public conference will be held on the campus of Xavier University, 3800 Victory Pkwy., Cincinnati, OH 45207, 513-745-3016.

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    FOR FURTHER INFORMATION CONTACT:

    For information regarding this notice: Gina Brackett, Food and Drug Administration, 6751 Steger Dr., Cincinnati, OH 45237, 513-679-2700, FAX: 513-679-2771, email: gina.brackett@fda.hhs.gov.

    For information regarding the conference and registration: Marla Phillips, Xavier Health, Xavier University, 3800 Victory Pkwy., Cincinnati, OH 45207-5471, 513-745-3073, email: phillipsm4@xavier.edu or visit http://www.XavierMedCon.com.

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    SUPPLEMENTARY INFORMATION:

    The public conference helps fulfill the Department of Health and Human Services' and FDA's important mission to protect the public health. The conference will provide those engaged in FDA-regulated medical devices (for humans) with information on the following topics:

    • Center Director Corner: Strategic Priorities for 2017 and Beyond.
    • European Union (EU) Regulations—Exploring the Unknown.
    • Impact of the New EU Regulations on Your Global Regulatory Strategy.
    • Digital Health—Key Focus Areas for FDA and Industry.
    • Office of Compliance Strategic Priorities.
    • Update from the Office of Device Evaluation.
    • FDA Insight on the 510(k) Modifications Guidance.
    • 510(k) Modifications: To submit or not to submit?
    • Your Contract Manufacturer Received a Warning Letter. What Now?
    • Defending Claims for Your Device.
    • The Impact of Cultural Misalignment . . . . and the Path Forward.
    • The Importance of Quality and Regulatory throughout the Merger and Acquisition Lifecycle—Landmines or Opportunities.
    • What to Expect with FDA's Program Alignment?
    • Investigator Insights and Breaking News.

    FDA has made education of the drug and device manufacturing community a high priority to help ensure the quality of FDA-regulated drugs and devices. The conference helps to achieve objectives set forth in section 406 of the Food and Drug Administration Modernization Act of 1997 (21 U.S.C. 393), which includes working closely with stakeholders and maximizing the availability and clarity of information to stakeholders and the public. The conference also is consistent with the Small Business Regulatory Enforcement Fairness Act of 1996 (Pub. L. 104-121) by providing outreach activities by Government Agencies to small businesses.

    Registration: There is a registration fee. The conference registration fees cover the cost of the presentations, training materials, receptions, breakfasts, and lunches for the 3 days of the conference. There will be onsite registration. The cost of registration is as follows:

    Table 1—Registration Fees1

    Attendee typeStandard rate
    Industry1,695
    Small Business (<100 employees)1,200
    Start-up Manufacturer$300
    Academic$300
    FDA/Government EmployeeFree
    1 The following forms of payment will be accepted: American Express, Visa, MasterCard, and company checks.

    To register online for the public conference, please visit the “Registration” link on the conference Web site at http://www.XavierMedCon.com. FDA has verified the Web site address, but is not responsible for subsequent changes to the Web site after this document publishes in the Federal Register.

    To register by mail, please send your name, title, firm name, address, telephone, email, and payment information for the fee to Xavier University, Attention: Marla Phillips, 3800 Victory Pkwy., Cincinnati, OH 45207-5471. An email will be sent confirming your registration.

    Attendees are responsible for their own accommodations. The conference headquarter hotel is the Downtown Cincinnati Hilton Netherlands Plaza, 35 West 5th St., Cincinnati, OH, 45202, 513-421-9100. Special Conference Block rates are available through April 11, 2017. To make reservations online, please visit the “Venue/Logistics” link at http://www.XavierMedCon.com. If you need special accommodations due to a disability, please contact Marla Phillips (see FOR FURTHER INFORMATION CONTACT) at least 7 days in advance of the conference.

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    Dated: March 29, 2017.

    Anna K. Abram,

    Deputy Commissioner for Policy, Planning, Legislation, and Analysis.

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    [FR Doc. 2017-06699 Filed 4-4-17; 8:45 am]

    BILLING CODE 4164-01-P

Document Information

Published:
04/05/2017
Department:
Food and Drug Administration
Entry Type:
Notice
Action:
Notice of public conference.
Document Number:
2017-06699
Dates:
The public conference will be held on May 3, 2017, from 8:30 a.m. to 5 p.m.; May 4, 2017, from 8:30 a.m. to 5 p.m.; and May 5, 2017, from 8:30 a.m. to 12:30 p.m.
Pages:
16599-16599 (1 pages)
Docket Numbers:
Docket No. FDA-2017-N-0001
PDF File:
2017-06699.pdf