Shows & Panels
- Accelerate and Streamline for Better Customer Service
- Ask the CIO
- The Big Data Dilemma
- Carrying On with Continuity of Operations
- Client Virtualization Solutions
- Data Protection in a Virtual World
- Expert Voices
- Federal Executive Forum
- Federal IT Challenge
- Federal Tech Talk
- Feds in the Cloud
- Health IT: A Policy Change Agent
- IT Innovation in the New Era of Government
- Making Dollars And Sense Out of Data Center Consolidation
- Navigating the Private Cloud
- One Step to the Cloud, Two Steps Toward Innovation
- Path to FDCCI Compliance
- Take Command of Your Mobility Initiative
Shows & Panels
John Gilroy hosts a roundtable discussion of mobile health applications and and how they can be certified to meet specific standards.
April 30, 2013
Sally Howard is stepping down as the chief of staff at Health and Human Services to become the deputy commissioner for policy at the Food and Drug Administration.
Tony Varano, founder and CEO of DSG, joins host John Gilroy to discuss how to improve healthcare data collection.
March 12, 2013
FDA Commissioner Hamburg says budget cuts mean fewer inspections, less safe food
The Food and Drug Administration's new Information Management Strategic plan is helping to create a new infrastructure to support using data to meet its mission.
January 24, 2013
Paul Strasser of Dynamics Research Corporation talks about a new deal his company has with FDA. Marilee Fitzgerald, director of the Department of Defense Education Activity, discusses promoting STEM fields. Tim Scannell of Technology Guide reports from the Consumer Electronics Show in Las Vegas.
Martin Libicki of Rand Corp talks about the 2013 Defense Authorization Bill. Dov Zakheim reviews what DoD Secretary-nominee Chuck Hagel can expect from Congress. Attorney Mark Schamel explains how the Defense Authorization Bill helps off-duty law enforcement agents. Erik Olson of the Pew Health Group discusses new food safety rules issued by the FDA. John Palguta of the Partnership for Public Service previews the SAMMIE nomination process. Katherine McFate discusses OMB Watch's name change.
The Food and Drug Administration on Friday proposed the most sweeping food safety rules in decades, requiring farmers and food companies to be more vigilant in the wake of deadly outbreaks in peanuts, cantaloupe and leafy greens.
The Food and Drug Administration said Monday it will collaborate with medical device manufacturers on a public-private partnership designed to speed up the development of new medical technology.
Lawrence Korb of the Center for American Progress says sequestration may not be such a bad thing. Buddy Bland talk about upgrades to the Oak Ridge National Laboratory's supercomputer. Mark Russo of the FDA talks about food shortages caused by Hurricane Sandy.
Sean Patton of Lockheed Martin talks about the EPA's migration to a collaboration and communication service. Sanjay Koyani discusses a partnership with the Centers for Disease Control and Prevention and other Health and Human Services components to get better leverage out of the information it has. Engineer Norman R. Augustin talks about a new report on STEM prepared by the National Academy of Engineering and the National Research Council.
Dr. Andrew Von Eschenbach of the Manhattan Institute's Project FDA explains how a legislative mandate does not come with the funding needed to implement it. And Acting Public Printer Davita-Vance Cooks lays out the five-year strategic plan as the Government Printing Offices faces a digital future.
Last year, the FDA proposed a policy to test apps that included "very high-risk interventions" that did not cause any unintended consequences. The agency is now expected to release final policy by the end of this year on which apps it will oversee.
A spending bill required to avoid a government shutdown at the end of the month has cleared a procedural hurdle in the Senate.
The CIO said he's using an agile approach to keep large programs on track and looking to the cloud to improve the agency's business processes.
Jul 19, 2012(Encore presentation August 27, 2012)
A Government Accountability Office report found the Department of Health and Human Services and the Environmental Protection Agency need to do a better job managing their employees under Title 42.
The Office of Special Counsel is reminding agencies not to target email monitoring of employees that could have a chilling effect on whistleblowers who report waste, fraud and abuse.
Avinash Kar of the Natural Resources Defense Council discusses an FDA decision on cattle feeding processes. Attorney Joseph Petrillo offers his perspective on burgeoning bid protests. GAO's Bill Woods talks about GSA's reliance on "dun" numbers. Jamison Cush discusses Microsoft's new tablet device. Charles Scoville works with amputee veterans.
The Food and Drug Administration would have more power to catch tainted pharmaceuticals manufactured overseas before they enter the U.S. market under legislation passed Wednesday by House lawmakers.
Dr. Kyle Myers works with a team of physicists, engineers and mathematicians, who apply their expertise to evaluating imaging systems that help diagnosis medical conditions such as cancer.