Defense Production Act

Defense Production Act

Defense Production Act

The Biden Administration has strongly signaled its intent to invoke the Defense Production Act (“DPA”) in a variety of contexts imminently to bolster the country’s response to the COVID-19 pandemic, specifically with respect to the manufacture and distribution of COVID-19 vaccines, tests, therapies, and other essential supplies. 

Indeed, on February 5, 2021, pursuant to the DPA, the Biden Administration expanded the priority rating of Pfizer’s vaccine production contract to ensure the company has first access to the filling pumps and tangential flow filtration skid units it needs to produce its COVID-19 vaccine.  The administration also indicated plans to exercise its DPA authorities to boost domestic manufacture of surgical gloves and at-home COVID-19 tests by investing in raw materials, additional production lines, and new manufacturing plants.  See King & Spalding blog post, “White House COVID-19 Response Team Discusses Use of DPA” (February 5, 2021). 

If invoked in other contexts, which is very likely, the DPA will significantly impact life science companies and others directly involved in the manufacture and distribution of COVID-19 vaccines, tests, therapies, and other essential supplies, as well as a wide range of other companies who buy and supply the components of such supplies for non-COVID-19-related purposes.

Resources:

COVID-19 Vaccine Rollout
COVID-19 Vaccine Updates

Counseled a leading international medical device company on Defense Production Act contract and rated order requests and associated compliance issues and commercial considerations.

Advised several life sciences companies on the operation and application of the Defense Production Act, the intersection between FDA regulatory requirements, federal contracting obligations, and the Defense Production Act, and the establishment and implementation of internal policies, procedures, and protocols pertaining to Defense Production Act contract and rated order requests and related compliance matters.

Counseled multiple life sciences companies on the implications of Defense Production Act invocation with respect to their suppliers and strategic supply chain and business impact planning.

Advised private equity and venture capital clients regarding the potential impact of funding received by portfolio companies under Title III of the Defense Production Act on CFIUS review of foreign investments.

Assisted a leading medical device manufacturer and global automaker with the establishment of manufacturing capabilities to respond to government contract requests for ventilators issued under the Defense Production Act.

Negotiated on behalf of a client a contract awarded under the Defense Production Act to supply the federal government with 150 million N95 respirator masks.

Assisted an international medical device manufacturer with the negotiation, execution, and implementation of a contract awarded under the Defense Production Act to supply the federal government with thousands of ventilators.

Advised an international aerospace and defense company navigate Defense Production Act contract and rated order requests in conflict with state shut- down orders.

Counseled a leading distribution and supply company in connection with contracts issued pursuant to the Defense Production Act.

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Counseled a leading international medical device company on Defense Production Act contract and rated order requests and associated compliance issues and commercial considerations.

Advised several life sciences companies on the operation and application of the Defense Production Act, the intersection between FDA regulatory requirements, federal contracting obligations, and the Defense Production Act, and the establishment and implementation of internal policies, procedures, and protocols pertaining to Defense Production Act contract and rated order requests and related compliance matters.

Counseled multiple life sciences companies on the implications of Defense Production Act invocation with respect to their suppliers and strategic supply chain and business impact planning.

Advised private equity and venture capital clients regarding the potential impact of funding received by portfolio companies under Title III of the Defense Production Act on CFIUS review of foreign investments.

Assisted a leading medical device manufacturer and global automaker with the establishment of manufacturing capabilities to respond to government contract requests for ventilators issued under the Defense Production Act.

Negotiated on behalf of a client a contract awarded under the Defense Production Act to supply the federal government with 150 million N95 respirator masks.

Assisted an international medical device manufacturer with the negotiation, execution, and implementation of a contract awarded under the Defense Production Act to supply the federal government with thousands of ventilators.

Advised an international aerospace and defense company navigate Defense Production Act contract and rated order requests in conflict with state shut- down orders.

Counseled a leading distribution and supply company in connection with contracts issued pursuant to the Defense Production Act.