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International Life Sciences Newsletter - Life Sciences Legal Lens Vol. 2

Update: AI-Enabled Medical Devices and IVDs Confirmed as “High-Risk”

Digital Omnibus Update. More time (up to August 2028) yet confirming that AI-enabled medical devices and IVDs stay subject to the AI Act.

2 July 2026
Briefing

by Irina Rebin

4 of 9 Insights

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International Life Sciences Newsletter - Life Sciences Legal Lens Vol. 2

CJEU on distributor's verification obligations under MDR

Medical device (and IVD) distributors. CJEU confirms that distributors need not repeat the manufacturer’s classification or conformity assessment, but must perform a “consistency check” for obvious inconsistencies.

1 July 2026
Briefing

by Irina Rebin

1 of 9 Insights

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Life sciences & healthcare

Landmark CJEU Decision on the Obligations of Medical Device Distributors

23 June 2026
Briefing

by Dr. Daniel Tietjen and Daniel Dietrich

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Life sciences & healthcare

CJEU Advocate General on Distributors’ Obligations for Medical Devices

29 April 2026
Briefing

by Dr. Daniel Tietjen and Daniel Dietrich

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ivdr mdr
International Life Sciences Newsletter - Life Sciences Legal Lens Vol 1

Proposed Amendments to the EU Medical Device Regulation

A European Perspective #1 | The Commission’s proposed MDR/IVDR reform introduces substantial changes to certification, classification and compliance frameworks. Medical device companies should assess potential im-pacts early and prepare for a shifting regulatory landscape.

15 April 2026
Briefing

by Bartosz Świdrak

2 of 9 Insights

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International Life Sciences Newsletter - Life Sciences Legal Lens Vol 1

The 2026 Pharma Package: A New Regulatory Framework for Medicinal Products in the EU

A European Perspective #1 | The EU’s largest pharmaceutical law reform in over 20 years introduces a new regulatory exclusivity framework, revised orphan drug incentives and an antimicrobial voucher. Strategic exclusivity planning will become essential for pharmaceutical companies.

15 April 2026
Briefing

by Irina Rebin

1 of 9 Insights

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International life sciences
International Life Sciences Newsletter - Life Sciences Legal Lens Vol 1

No claim for damages as a result of participation in clinical drug trials

A European Perspective #1 | GERMANY | The Frankfurt am Main Regional Court confirms: No reduction in the burden of proof (presumption of causality) pursuant to Section 84 (2) of the German Medicines Act (AMG) for IMP (not even by analogy) and no liability on the part of the sponsor in the event of (insufficient) risk information provided by the investigating physician.

1 April 2026

by Irina Rebin

7 of 9 Insights

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International life sciences
International Life Sciences Newsletter - Life Sciences Legal Lens Vol 1

Promotional activities for medical devices may qualify as agency even without direct negotiation power

A European Perspective #1 | FRANCE | The French Supreme Court confirms a broad interpretation of commercial agent status. A key ruling increasing requalification risks and potential termination indemnity exposure for manufacturers and distributors.

1 April 2026
Briefing

by Annabelle Lebaudy

6 of 9 Insights

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Brands & advertising

Retailer obligations under scrutiny: ECJ to clarify scope of inspection obligations

13 November 2025
In-depth analysis

by Dr. Wiebke Baars, LL.M.

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