EuroNews (English)

Commission seeks faster approvals for biotech products

- Marta Iraola Iribarren

The European Commission presented a series of actions to boost biotechnol­ogy and biomanufac­turing in the EU, confirming a leak published by Euronews earlier this week.

As previously reported, the Commission is planning to assess the current rules for biotech products market approval in a bid to make the EU regulatory framework and its implementa­tion smoother.

“What we hear from industry is that there are indeed huge difference­s, in what time it takes to have a product that is finalised and tested from the side of the business to being able to market it,” Vestager explained presenting the proposal.

“The claim is that in the US you can do that in two to three years, but within the European Union, it will take you six to eight years,” she continued.

Vestager mentioned the approval process of COVID-19 vaccines as an example of what could also work for biotech products.

“The reason why we could do it in record time [the approval of the vaccines] was that instead of waiting for all the tests to be finalised, and then all of that data being sent to us, we asked the businesses to send us their results in real-time so that it could be assessed in real-time,” she said.

In this way, while companies are conducting final tests, regulatory authoritie­s can prepare final approvals without compromisi­ng safety.

In reaction to the proposal, the EU’s largest biotech associatio­n EuropaBio stressed the importance of rapidly addressing regulatory challenges in a statement.

“If Europe is to succeed, this initiative has to rapidly transform ‘rhetoric’ into policy and legislativ­e action for competitiv­eness, enabling innovators to thrive and grow, and creating long-term investment into infrastruc­tures, employment and skills in Europe,” the statement said.

The European Federation of Pharmaceut­ical Industries (EFPIA) said that the commission’s strategy “should include coordinate­d and strategic governance to ensure policy coherence and to bridge existing silos between research, health, industry, and internal market policies”.

 ?? ?? New Commission plan for the future of the biotech sector in Europe lies in the simplifica­tion of the regulatory process.
New Commission plan for the future of the biotech sector in Europe lies in the simplifica­tion of the regulatory process.

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