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COVID-19 Liability Immunity - What You Need to Know Now

The Secretary of the Department of Health and Human Services issued a declaration1 providing liability immunity to certain individuals and entities against covered claims of loss relating to the manufacture, distribution, administration, or use of medical countermeasures (“Covered Countermeasures”), except for claims involving “willful misconduct.”

The COVID-19 Declaration was issued on March 10, 2020 under the authority of the Public Readiness and Emergency Preparedness Act of 2005 (“PREP Act”), codified at 42 U.S.C. §247d-6d, and is retroactively effective beginning February 4, 2020.  

Who is this primarily relevant to?

Manufacturers, distributors, program managers, “qualified persons” and their officials, agents, and employees authorized to prescribe, administer, deliver, distribute or dispense any antiviral, drug, biologic, or vaccine used to treat, diagnose, cure, prevent, or mitigate COVID-19, the transmission of SARS-CoV-2, or a virus mutating therefrom, or “any device used in the administration of any such product, and all components and constituent materials of any such product.”

Who is a “qualified person”?

Any person authorized to prescribe, administer, deliver, distribute or dispense the Covered Countermeasures.

What is the purpose of the COVID-19 Declaration? 

To permit the special use of drugs and other medical products during the COVID-19 pandemic that either have not yet been approved/cleared by the FDA or may be used off-label without the risk of liability in the event of a covered injury or loss. Under the PREP Act, if there are injuries as a result of Covered Countermeasures relating to a public health emergency, the relief available can be found via the Countermeasures Injury Compensation Program (“CICP”), which is charged with establishing a fund for such injuries. 

What activities are covered?

Manufacturing, testing, development, distribution, administration, and use of the Covered Countermeasures.

When did it go into effect and how long does it last?

Effective as of February 4, 2020 through October 2024, unless extended. 

What are Covered Countermeasures?

Anything used against the pandemic or against adverse events from these products, including antivirals, drugs, biologics, diagnostics, devices, vaccines used to treat, diagnose, cure, prevent, or mitigate COVID-19, or the transmission of SARS-CoV-2 or a virus mutating therefrom, or any device used in the administration of any such product, and all components and constituent materials. 

Must be a qualified pandemic or epidemic product authorized for investigation or emergency use as defined in the PREP Act, the Food and Drug Cosmetic Act (“FDCA”), and the Public Health Service Act (“PHSA”). 

What are the key limitations/qualifications on immunity protection?

  1. Some form of premarket approval is required. The Covered Countermeasure must be approved or cleared by the FDA under the FDCA; licensed under the PHSA; or authorized for emergency use by the FDA under applicable provisions of the FDCA.
     
  2. Must be qualified pandemic or epidemic products, security countermeasures, or drugs, biologics, or devices authorized for emergency or investigational use. 
     
  3. Only for “recommended activities” involving Covered Countermeasures related to present or future federal contracts or other federal transactions or agreements, or activities authorized by authorities with jurisdiction to prescribe, administer, deliver, distribute, or dispense Covered Countermeasures following an emergency declaration.
     
  4. Does not apply to death or serious physical injury caused by willful misconduct.
     
  5. Not available for foreign claims. 
     
  6. Claim must arise from conduct that is directly related to the development/distribution of a Covered Countermeasure.  

Does my product qualify for immunity protection?

This will likely depend on whether the product is authorized for use in connection with the COVID-19 pandemic.   

Who has “authority” in connection with the pandemic?

The COVID-19 Declaration broadly defines those with “authority” in connection with the pandemic to include “the public agency or its delegate that has legal responsibility and authority for responding to an incident based on political or geographical (e.g., city, county, tribal, state or federal boundary lines) or functional (e.g., law enforcement, public health) range or sphere of authority.” 

Could this provide liability immunity for my clinical trial?

Yes, as long as you meet the other requirements. 

Are there any claims not covered by the COVID-19Declaration? 

Yes, claims for “willful misconduct,” which require more than reckless or negligent behavior. To prove, the PREP Act requires clear and convincing evidence of an act or failure to act that is taken (1) intentionally to achieve a wrongful purpose; (2) knowingly without legal or factual justification; and (3) in disregard of a known of obvious risk that is so great as to make it highly probable that the harm will outweigh the benefit. 

Is there a geographic limitation? 

No. However, immunity is not available for foreign claims.

What is the authority for the COVID-19 Declaration?

The PREP Act, 42 U.S.C. § 247d-6d.

Is there precedent supporting this immunity?

Yes, see, e.g., Parker v. St. Lawrence County Pub. Health Dept., 102 A.D.3d 140 (3rd Dep’t 2012) (finding federal preemption over Plaintiff’s state law claim based on the unconsented vaccination of a minor during the H1N1 epidemic).

How does the COVID-19 Declaration compare to prior declarations?

Overall, the COVID-19 Declaration follows a similar framework as previous PREP Act declarations issued in response to Ebola, Zika, influenza, anthrax, botulinum, and smallpox over the past decade.   

Referred to herein as the “COVID-19 Declaration.”  See 85 FR 15198 (available at https://www.federalregister.gov/documents/2020/03/17/2020-05484/declaration-under-the-public-readiness-and-emergency-preparedness-act-for-medical-countermeasures). 

Copyright © 2020 Womble Bond Dickinson (US) LLP All Rights Reserved.

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About this Author

Kelley P. Doran Government Contracts Attorney Womble Bond Dickinson Washington, D.C.
Partner

For over 20 years, Kelley has focused his practice on government contracts counseling, negotiations and litigation, representing a broad range of domestic and foreign commercial item, defense and homeland security contractors that sell products and services to federal, state and local governments. He has worked with companies in such industries as life sciences, information technology, cybersecurity, homeland security and defense and aerospace. Kelley has developed a particular focus on biodefense and pandemic influenza preparedness and regularly advises clients regarding contracts and...

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Sara Tucker Complex Products Liability Litigation Attorney Womble Bond Dickinson Atlanta, GA
Partner

Sara Tucker concentrates her practice on complex products liability litigation with a focus on pharmaceutical and medical device litigation.  A veteran trial lawyer, Sara has experience defending clients in high-stakes mass tort and multi-district cases in federal and state courts.  She also has experience in consolidated state court litigation, consumer class actions and medical malpractice.

The American Bar Association’s Young Lawyers Division selected Sara for its “On the Rise – Top 40 Young Lawyers” award in 2019, and Georgia Super Lawyers magazine has recognized Sara as a Rising Star for each of the past five years. 

Experience 

  • Counsel for pharmaceutical company in multidistrict litigation (MDL) involving proton-pump inhibitor (PPI) medications.
  • Counsel for global medical technology company in cases alleging bacterial contamination of sterile syringes.
  • National trial team member for global medical device company related to inferior vena cava (IVC) filters.
  • National trial team member for global medical device company in both MDL as well as state court litigation involving hernia mesh products.
  • Counsel for medical device company in cases alleging death and /or paralysis related to surgically implanted medical devices.
  • Counsel for pharmaceutical company in MDL litigation relating to chemotherapy medications.
  • Trial team member for one of the world’s largest medical device companies involving allegations of negligence in the design of a laser-resistant endotracheal tube. The client was assessed zero liability despite jury verdict of $18 million awarded against co-defendant health care providers.
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Suzanne B. Boehm Government Contracting Attorney Womble Bond Dickinson Washington, D.C.
Associate

*Ms. Boehm is not admitted to practice law in the District of Columbia. She is being supervised by a licensed District of Columbia Bar member.

Suzanne provides a multidimensional understanding of the Government procurement process and valuable insight into effective contract negotiation, administration, and litigation strategy. Suzanne formerly served as Assistant Counsel for the Defense Logistics Agency Energy (“DLA Energy”), advising on all aspects of energy-related defense acquisitions under the multifaceted framework of the Federal Acquisition Regulation (“FAR”) and...

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