Skip to nav Skip to content

Science Speaks

Blog Home

COVID-19: HHS explains “Operation Warp Speed”

Daniel R. Lucey, MD, MPH, FIDSA
Facebook Twitter LinkedIn Email

On Friday, The U.S. Department of Health and Human Services posted a succinct 4-page document titled “Explaining Operation Warp Speed."

The summary begins by answering three questions: What is the goal [of OWS]? How will the goal will be accomplished? Who is working on OWS? It moves to an informative chronology of specific amounts of funding (16 specific bulleted items) for three aspects of COVID Vaccines (and one antiviral antibody): Development, manufacturing, and distribution. The update ends with answers to three questions: Who’s leading Operation Warp Speed? What are you doing to make these products affordable for Americans?  How is Operation Warp Speed being funded?

In my opinion, a few of the key points in this excellent summary include:

  • “Operation Warp Speed (OWS) aims to begin delivery of 300 million doses of a safe, effective vaccine for COVID-19 by January 2021, as part of a broader strategy to accelerate the development, manufacture, and distribution of COVID-19 vaccines, therapeutics, and diagnostics (collectively known as countermeasures”).

(My note: Thus, OWS is not solely focused on vaccines.)

  • “The Administration is committed to providing free or low-cost COVID-19 countermeasures to the American people as fast as possible. Any vaccine or therapeutic doses purchased with US taxpayer dollars will be given to the American people at no cost.”

(My note: A crucial commitment regarding “no cost” to Americans for vaccines or therapeutics “purchased with US taxpayer dollars.”)

  • “HHS Secretary Alex Azar and Defense Secretary Mark Esper oversee OWS, with Dr. Moncef Slaoui designated as chief advisor and General Gustave F. Perna confirmed as chief operating officer. To allow these OWS leaders to focus on operational work, in the near future the program will be announcing separate points of contact, with deep expertise and involvement in the program, for communication with Congress and the public”.

(My note: Of particular interest will be the spokesperson(s) for explaining the anticipated COVID-19 vaccine Emergency Use Authorization consideration by the FDA.  As noted in the July 31 IDSA Science Speaks post, the only vaccine having ever received FDA EUA was the (approved) anthrax vaccine for 12 months only from 2005-2006 to be used by the Department of Defense.   The rationale is provided in this 2005 Federal Register document.) 

Loading...

This website uses cookies

We use cookies to ensure that we give you the best experience on our website. Cookies facilitate the functioning of this site including a member login and personalized experience. Cookies are also used to generate analytics to improve this site as well as enable social media functionality.