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Welcome to the July 2019 edition of our newsletter. The EMEA Healthcare Industry Group Newsletter is your regular digest of legal developments affecting the life science and healthcare industries across the region.

In this Issue:

Europe

  • New EU measures boost the generic pharmaceuticals industry
  • Falsified drugs from Italy reach UK patients five months after the EU Falsified Medicines Regime went live

Europe – Brexit

  • EMA settles into its new Dutch home whilst still battling its UK tenancy obligations in the courts Dutch relocation
  • Brexit Select Committee Hearing – impact on the pharmaceuticals industry
  • LRQA withdraws Notified Body services: is the industry ready for the MDR / IVDR and a no-deal Brexit?

Germany

  • Apps on prescription?

Italy

  • New decree on clinical trials approved
  • Council of State rules in favour of public hospital in medical equipment tender case
  • Council of State dismisses biomedicine company’s tender appeal over latest generation devices
  • The exclusion of a medicinal product from a tender is legitimate when the same product is only relevant for its “off-label” use

Kazakhstan

  • Kazakhstan adopts Ethical Rules for the promotion of pharmaceutical products and medical devices

Poland

  • Joint initiative of V4 and Lithuania for fair prices of medicine
  • Amended regulations regarding the opinion on purposefulness of healthcare investments

Russia

  • New law empowers government to require drug price reductions
  • Further development of the track-and-trace serialisation system in Russia

Spain

  • New guide on advertising to the general public medicines for human use not subject to medical prescription

Turkey

  • Turkey introduces changes to clinical trial applications
  • Cosmetics safety: Turkey continues cracking down on unsafe and noncompliant cosmetic products

UK

  • Legal basis for processing personal data in clinical trials – what’s the right approach?
  • NHS Digital’s new Internet First Policy
  • Simplified hospital credentialing process for Medtech industry staff: MIA and LSI combine operations
Author

Julia joined Baker McKenzie's London office as a trainee in 2005, qualifying in 2007, with a secondment to the Singapore office, and has shaped her practice to focus exclusively on regulatory matters affecting the Healthcare & Life Sciences industry.

Author

Els Janssens is a Counsel in commercial law, litigation and healthcare regulatory issues in the Brussels office. Els worked as a senior regulatory legal counsel for Johnson & Johnson supporting the company's global safety operations and advising on regulatory issues in relation to specific medicinal products. Els also worked as legal advisor in the European Medicines Agency where she advised management, scientific committees, CMD(h) and the European Commission on a wide variety of issues in connection with authorisation procedures, submission requirements, pharmacovigilance obligations and procedures as well as inspections. Based in Abu Dhabi from 2014 to 2019, she advised both multinational medical devices and pharmaceutical clients on healthcare regulations in the EU and UAE.