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Posts with tag EU
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EMA’s envisaged risk-based and human-centric approach to regulate AI
Bird & Bird’s international life sciences and healthcare team is at the forefront of the legal developments with regard to AI and the life sciences sector. This article is part of our new series, which will highlight different legal angles to consider when implementing AI in the life sciences and healthcare industry.
Artificial Intelligence (“AI”) has emerged as a transformative force in the healthcare industry, and its significance for the pharmaceutical sector is particularly profound....
September 14, 2023
6 min read
EU Commission’s proposed changes to marketing authorisation...
This article is part of a series that covers the proposed...
August 9, 2023
6 min read
Code of practice introduced for holding cultivated...
Particularly in the Netherlands, developments in the field of...
July 12, 2023
6 min read
Reform of the EU pharmaceutical legislation: proposals...
This article is part of a series that covers the proposed...
July 10, 2023
4 min read
Increased interest in the use of psychedelics as mainstream therapies
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July 4, 2023
6 min read
Proposed reform of the EU pharmaceutical legislation: New regime for orphan medicinal products under the proposed regulation
This article is part of a series that covers the proposed reforms to EU pharmaceutical legislation....
June 27, 2023
4 min read
Strengthened Environmental Risk Assessment requirements under the proposed new directive on medicinal products for human use
This article is part of a series that covers the proposed reforms to EU pharmaceutical legislation....
June 23, 2023
3 min read
European Commission proposes to change the rules on regulatory data protection for medicines
This article is part of a series that covers the proposed reforms to EU pharmaceutical legislation....
June 15, 2023
4 min read
A Guide to the UPC and the UP
The opening of the Unified Patent Court (UPC) on 1 June 2023 may be the most significant development...
June 9, 2023
2 min read
Proposed updates to the regulation of medical devices
While it might be challenging for manufacturers of medical devices to navigate the evolving regulations...
May 10, 2023
3 min read