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Insights and Analysis

Q3/2024 Life Science Law Update – Key developments for pharma & device companies in EU

31 October 2024
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Insights and Analysis
Q3/2024 Life Science Law Update – Key developments for pharma & device companies in EU
Chapter
  • Chapter

  • Chapter 1

    Life Sciences Regulatory
  • Chapter 2

    Corporate Governance & Corporate Social Responsibility
  • Chapter 3

    Anti-Bribery and Anti-Corruption
  • Chapter 4

    Competition and Antitrust
  • Chapter 5

    Intersection of Life Science and Data Privacy
  • Chapter 6

    Data Privacy

Key takeaways

Pharma: Revision of the Urban Wastewater Treatment Directive; new guidance on validity of clinical studies for Joint Clinical HT Assessments; Initiatives to improve cancer treatments; etc.

Devices: Amendment of MDR and IVDR re supply disruptions;

Corporate: CSDDD entered into force; etc.

Compliance: Transparency in pharmaceutical pricing; Combating corruption; etc.

Competition: New Corporate Commissioner; Draft guidelines addressing exclusionary conduct and abuse of dominance launched; etc.

Intersection of Life Science and Privacy: AI Act entered into force

Data Privacy: Decision on the interpretation of data concerning health; etc.

The Q1 and Q3 Life Science and Health Care Law Update covers key trends in the EU only while the other reports (on Q2 and Q4) cover key trends in the EU as well as in the Big Five (France, Germany, Italy, Spain, UK) in life sciences regulatory, corporate, compliance, competition, and privacy.

Chapter 1

1

Life Sciences Regulatory

expanded collapse

Pharma updates

  • Revision of the Urban Wastewater Treatment Directive (UWWTD): The UWWTD aims to address emerging pollutants like pharmaceuticals, microplastics, and endocrine disruptors, which were not covered by the original directive. It mandates urban wastewater collection and treatment to better protect human health and the environment. An extended producer responsibility scheme requires pharmaceutical and cosmetic producers to cover at least 80% of the costs for removing micropollutants from wastewater. The Directive must be implemented by the Member States with deadlines ranging between 31 December 2033 and 31 December 2045. However, given the future cost burden we already see clients assessing the impact.
  • Commission publishes new guidance on validity of clinical studies for Joint Clinical Assessments under the EU Health Technology Assessment Regulation (HTAR): This framework aims to enhance the availability of innovative health technologies, such as medicines and medical devices, for EU patients while reducing duplication of efforts among national HTA authorities and industry.
  • Improved access to cancer medicines: A new OECD's analysis addresses challenges in ensuring equal access to cancer medicines within health systems. It suggests stimulating competition among oncology drug producers to create budget savings, which could be reinvested in new, beneficial treatments.
  • Dutch EUR 2 Billion Initiative to boost Cancer Treatment Supply: The European Commission approved a EUR 2 billion Dutch measure to support the PALLAS project, led by the Nuclear Research and Consultancy Group. The project aims to produce medical radioisotopes for cancer diagnosis and treatment, contributing to the EU's Pharmaceutical Strategy by ensuring a secure supply of essential medicines. It involves building nuclear health center for processing medical isotopes into radio chemicals and radiopharmaceuticals.

Device updates

  • Regulation amending MDR and IVDR published: On 9 July 2024, the Regulation (EU) 2024/1860 amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards a gradual roll-out of Eudamed, the obligation to inform in case of interruption or discontinuation of supply, and transitional provisions for certain in vitro diagnostic medical devices was published on the Official Journal of the European Union.

Authors: Joerg Schickert, Caroline Schmalenbach, Fabien Roy, Anastasia Vernikou

Keen to dive deeper into the latest European pharma and devices regulatory updates? Contact Joerg Schickert to subscribe to a more detailed quarterly report.

Chapter 2

2

Corporate Governance & Corporate Social Responsibility

expanded collapse

The Corporate Sustainability Due Diligence Directive (CSDDD) entered into force on 25 July 2024: Member States are required to implement it by 26 July 2026. It applies to large EU companies (1,000+ employees and over €450 million in turnover) and certain non-EU companies. The CSDDD mandates a risk-based human rights and environmental due diligence process and a climate transition plan. Non-compliance can result in penalties, public naming, civil liability for damages, and requirements to disclose evidence for legal actions, including actions initiated by trade unions or NGOs on behalf of affected parties.

Authors: Lutz Angerer, Thomas Weber

For a more in depth quarterly update on corporate governance & corporate social responsibility contact Joerg Schickert to subscribe to a more detailed report.

 

Chapter 3

3

Anti-Bribery and Anti-Corruption

expanded collapse
  • Update on the legislative procedure of the Directive on combating corruption: The legislative procedure for the Directive on combating corruption is advancing, following the Council of the European Union's agreement, to establish unified minimum standards across Member States. The European Parliament must now confirm its position before trilogue negotiations can take place to finalize the proposal, replacing existing separate laws.

  • Push for greater transparency in pharmaceutical pricing: An OECD report published on 11 September 2024, emphasizes the need for greater transparency in pharmaceutical pricing, following the 72nd World Health Assembly and the Oslo Medicines Initiative. The report explores which medicine prices should be disclosed and assesses the feasibility of sharing price information across OECD countries. It finds a significant interest among member countries in sharing net pharmaceutical prices through a closed network, with many expressing willingness to participate in a pilot program for this purpose.

Authors: Joerg Schickert, Caroline Schmalenbach

Want a more detailed quarterly update on anti-bribery and anti-corruption? Contact Joerg Schickert to subscribe to receive more in-depth content. 

Chapter 4

4

Competition and Antitrust

expanded collapse
  • Teresa Ribera has been appointed as the new Competition Commissioner: European Commission President von der Leyen's outlines in her Mission Letter expectations for Ribera to modernize competition policy, particularly regarding merger control and challenges faced by SMEs, especially concerning foreign "killer acquisitions." The letter emphasizes strengthening the enforcement of competition rules related to state aid, foreign subsidies, anticompetitive agreements, and abuse of dominance.

  • The European Commission launched a consultation draft on 1 August 2024 on guidelines addressing exclusionary conduct and abuse of dominance: These guidelines define concepts such as dominance and exclusionary effects, categorizing conduct into various groups. The Commission may presume exclusionary effects in cases of exclusive dealing or predatory pricing. For “naked restrictions”, where a dominant company makes payments conditional on the delay or withdrawal of competing products, exclusionary effects are almost always assumed. For other types of behavior, a thorough examination is required to determine whether they restrict competition on the merits and cause exclusionary effects.

Authors: May Lyn Yuen, Falk Schöning

For a more in depth competition and antitrust update contact Joerg Schickert to subscribe to our detailed quarterly report.

Chapter 5

5

Intersection of Life Science and Data Privacy

expanded collapse
  • European Artificial Intelligence (AI) Act enters into force on 1 August 2024: The AI Act aims to ensure that AI systems in the EU are safe and uphold fundamental rights. It will be fully applicable 24 months after this date, while prohibitions on certain AI systems will be enforceable after six months. Regulations for general-purpose AI will take effect in 12 months, and the Commission aims to finalize the Code of Practice by April 2025. Key current action to take for our clients is to ensure to be aware when they use AI in their organization and to assess their legal role and risk level – and then act with a view to the AI Act coming into force.

Authors: Stefan Schuppert, Joerg Schickert, Theresa Mengler, Carolin Schmalenbach

For a more in depth competition and antitrust update contact Joerg Schickert to subscribe to our detailed quarterly report.

Chapter 6

6

Data Privacy

expanded collapse
  • European Commission publishes FAQ on Data Act on 6 September 2024: The Data Act aims to ensure fairness in data value distribution and will take effect on September 12, 2025. The FAQs clarify key provisions, including the relationship between the Data Act and GDPR, access to IoT data, roles of users and data holders, and unfair practices in B2B data-sharing contracts.

  • CJEU publishes decision on the interpretation of data concerning health: On 4 October 2024, the European Court of Justice (CJEU) ruled in Case C-21/23 that customer data collected by pharmacists, including names, addresses, and information for ordering non-prescription medicines online, qualifies as "health data" under the GDPR. This decision contradicts the Advocate General's opinion, stating that data can be classified as health data if the health of the individual can be inferred through association or deduction.

Authors: Stefan Schuppert, Theresa Mengler

Eager to deep dive into the latest data privacy and other trends discussed in this report? Contact Joerg Schickert to subscribe to a more in depth quarterly report

Contacts

bio-image

Dr. Jörg Schickert

Partner

location Munich

email Email me

bio-image

Fabien Roy

Partner

location Brussels

email Email me

bio-image

Dr. Lutz Angerer, LL.M. (University of Virginia)

Partner

location Munich

email Email me

bio-image

Dr. Falk Schöning

Partner

location Brussels, Berlin

email Email me

bio-image

Dr. Stefan Schuppert, LL.M. (Harvard)

Partner

location Munich

email Email me

bio-image

May Lyn Yuen

Partner

location Brussels

email Email me

bio-image

Thomas Weber

Counsel

location Munich

email Email me

bio-image

Theresa Mengler

Senior Associate

location Dusseldorf

email Email me

bio-image

Caroline Schmalenbach

Associate

location Hamburg

email Email me

bio-image

Anastasia Vernikou

Associate

location Brussels

email Email me

View more

Related topics

  • Cell, Tissue, and Gene Therapies (CTGT)
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  • Digital Health
  • Emerging Companies and Investors
  • Hospitals and Health Care Providers
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  • Life Science Government Enforcement and Compliance
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  • Health Compliance, Fraud and Abuse
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  • Advertising and Promotion of Pharmaceuticals and Biotechnology
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  • Regulatory Exclusivities, Hatch-Waxman, and Similar Statutes
  • Regulatory Inspections and cGMP
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Related keywords

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