Home > Transparency Posts > Upcoming Event: FDA Public Webinar About the “510(k) Premarket Review Process” and the “Use of Science in Regulatory Decision Making” Draft Reports, Tuesday, August 31, 1:00 p.m. ET

Upcoming Event: FDA Public Webinar About the “510(k) Premarket Review Process” and the “Use of Science in Regulatory Decision Making” Draft Reports, Tuesday, August 31, 1:00 p.m. ET

FDA recently published two preliminary reports conducted by the Center for Devices and Radiological Health (CDRH).  The first preliminary report is an assessment of the process used to review certain medical device applications before they are marketed (known as the 510(k) process) and draft recommendations.  The second preliminary report is an assessment of the use of science in CDRH's regulatory decision making and draft recommendations.  This is the first step in determining what, if any, improvements to these processes FDA may implement.

Next week, FDA is hosting a webinar where CDRH officials will discuss the details of both reports.  There will be an opportunity to ask questions.

The live webinar will be held on Tuesday, August 31, at 1:00 p.m. ET.

There are a limited number of spots available for the webinar.  Click here for more information about the webinar, which includes a link to join the webinar on August 31.

FDA is also soliciting comments from the public on the draft reports via www.regulations.gov, docket number FDA-2010-N-0348.

Afia Asamoah, Transparency Initiative Coordinator

  1. Jumper Rental
    August 30, 2010 at 6:20 pm

    Thanksfor posting the news about http://www.regulations.gov I’m excited that we have a chance to voice our comments and concerns.

  2. mark
    August 31, 2010 at 11:22 pm

    :( I thought it was tommorow, I can on here and realized I missed it

  3. Feromonas
    July 6, 2011 at 2:25 pm

    Im sorry I missed this

  4. November 23, 2011 at 6:16 pm

    I missed it too!

  5. Fooball Online
    January 6, 2012 at 1:41 pm

    Yes I missed too

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