European Commission–AstraZeneca COVID-19 vaccine dispute

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European Commission–AstraZeneca COVID-19 Vaccine Dispute

The European Commission–AstraZeneca COVID-19 Vaccine Dispute refers to a series of legal and contractual disagreements between the European Commission and the pharmaceutical company AstraZeneca regarding the supply and delivery of the COVID-19 vaccine developed by AstraZeneca in collaboration with the University of Oxford. The dispute highlights the challenges and tensions in global vaccine distribution during the COVID-19 pandemic.

Background[edit | edit source]

In August 2020, the European Commission, on behalf of the European Union (EU) member states, entered into an Advance Purchase Agreement (APA) with AstraZeneca for the supply of 300 million doses of its COVID-19 vaccine, with an option for an additional 100 million doses. This agreement was part of the EU's strategy to secure access to COVID-19 vaccines for its population.

Dispute[edit | edit source]

The dispute began in January 2021 when AstraZeneca announced a significant reduction in the number of vaccine doses it would be able to deliver to the EU in the first quarter of 2021, citing production issues at its European plants. The European Commission accused AstraZeneca of breaching its contractual obligations, arguing that the company should use its UK production sites to make up for the shortfall in the EU supply.

AstraZeneca countered that the contract contained a "best-effort" clause, meaning it was only required to make its best efforts to meet the delivery targets, rather than guaranteeing delivery by a specific date. The company also argued that the UK government had signed a contract with AstraZeneca three months before the EU did, which included terms that prioritized supply to the UK.

Legal Proceedings[edit | edit source]

In response to the delivery delays, the European Commission launched legal action against AstraZeneca in April 2021. The Commission sought a court order to compel AstraZeneca to deliver the remaining doses outlined in the APA by the end of June 2021. The legal proceedings were initiated in a Belgian court, as the APA specified that any disputes would be resolved under Belgian law.

Resolution[edit | edit source]

The dispute was partially resolved in September 2021 when the European Commission and AstraZeneca reached a settlement. Under the terms of the settlement, AstraZeneca committed to deliver an additional 200 million doses of its COVID-19 vaccine to the EU by the end of March 2022. This was in addition to the doses AstraZeneca had already delivered or was scheduled to deliver under the original APA.

Impact[edit | edit source]

The European Commission–AstraZeneca COVID-19 Vaccine Dispute had several implications. It exposed the vulnerabilities in the global vaccine supply chain and highlighted the challenges of vaccine nationalism. The dispute also underscored the importance of clear and enforceable contracts in securing vaccine supplies during a global health crisis. Furthermore, it prompted the EU to revise its vaccine procurement strategy, including more stringent contract terms and increased transparency in vaccine delivery schedules.

See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD