The American Chamber of Commerce to the EU (AmCham EU) fully recognises the pressure on public authorities in the EU and around the world to ensure timely access to COVID-19 vaccines. A strong economic recovery – and the return to normal life – relies on global access to vaccinations in a timely manner. Striving for this shared goal, stakeholders from both the public and private sectors are collaborating intensely to resolve the rapidly-evolving situation around the supply of vaccines.
International cooperation critical to ensure global access to COVID-19 vaccines
The American Chamber of Commerce to the EU (AmCham EU) fully recognises the pressure on public authorities in the EU and around the world to ensure timely access to COVID-19 vaccines. A strong economic recovery – and the return to normal life – relies on global access to vaccinations in a timely manner. Striving for this shared goal, stakeholders from both the public and private sectors are collaborating intensely to resolve the rapidly-evolving situation around the supply of vaccines.

AmCham EU is concerned that recent moves on export controls will fall short of their intended objectives. These measures risk disturbing the tightly calibrated and highly integrated supply chains used for the manufacturing and distribution of vaccines to patients globally. This can cause a ripple effect. In addition, restricting exports may spark retaliation from international partners, leading to further interruptions and ultimately hindering supply.
Putting an end to the COVID-19 crisis will only be possible through global cooperation. We encourage the EU, its Member States and other governments to increase collaboration as well as intensify the ongoing dialogue and partnership with industry. This will be critical in ensuring global access to COVID-19 vaccines and in mitigating the impact of the pandemic on the well-being of citizens and our economies.
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Healthcare, competitiveness, innovation and simplification
Europe’s life sciences sector sits at the heart of the EU’s competitiveness agenda. It supports advanced manufacturing and helps bring new treatments and technologies to patients. Yet companies deciding where to invest need a regulatory environment that is predictable and open to global cooperation.
The European Commission’s work on the Biotech Act and the targeted revision of the Medical Devices and In Vitro Diagnostics Regulations (MDR/IVDR) offers an opportunity to improve that environment. Both files can help make Europe a stronger location for life sciences investment.
The EU should use this moment to build a framework that keeps pace with scientific progress. That means faster and clearer procedures. It also means better use of data and intellectual property rules that recognise the realities of global supply chains.
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Strengthening EU competitiveness through an adaptive MDR/IVDR framework
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A global approach to strengthening Europe’s biotechnology ecosystem
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