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UK and EU life sciences update: AG opinion on SPC excipients; UK blocking order against counterfeiters; EU Biotech Act I GMMs mandate; DHSC branded medicines payment rate; MHRA AI findings

Published on: 18 June 2026

Published by an LexisNexis Life Sciences expert
Legal News
Table of contents
  • Intellectual property
  • Advocate General’s Opinion on whether excipients are active ingredients under the SPC Regulation (Halozyme, Inc v Czech IPO CJEU Case C-456/24)
  • Disputes and regulatory enforcement
  • Novo Nordisk wins blocking order in UK to combat counterfeit drugs
  • Commercialisation
  • DHSC publishes consultation outcome on statutory scheme headline payment percentage for branded medicines
  • Pharmaceuticals—regulatory framework
  • Council of the EU agrees mandate on European Biotech Act I directive on GMMs and organ processing
  • Irish Presidency of Council of the EU publishes programme for July to December 2026
  • Medical devices
  • More sections of this document available when you sign-in to Lexis+ or register for a free trial.

Article summary

Life Sciences weekly highlights

This week’s Life Sciences weekly highlights features Venner Shipley LLP’s legal analysis of the Advocate General’s view that a substance expressly designated as an excipient within the marketing authorisation cannot amount to a protected active ingredient under the SPC regime in Halozyme v Czech IPO case...

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