Skip to main content Skip to search Skip to main navigation

EC: Proposal for the Critical Medicines Act

The European Commission (EC) has proposed the Critical Medicines Act to enhance the availability of essential medicines in the EU. The regulation aims to diversify supply chains, boost EU pharmaceutical production, and improve access to critical medicines.

The Act responds to medicine shortages caused by supply chain vulnerabilities, global competition, and manufacturing issues. It provides an industrial toolkit to make the EU more attractive for pharmaceutical production and strengthen resilience. Key measures include:

  • Strategic Projects to expand or modernise EU manufacturing, supported by faster funding access and streamlined regulations.
  • State aid guidance to help Member States finance these projects.
  • Public procurement rules requiring diversified supply sources and incentives for EU production.
  • Collaborative procurement to improve medicine availability across the EU.
  • International partnerships to reduce dependence on limited suppliers.

This initiative complements the EU pharmaceutical reform and EMA’s expanded role in managing shortages, reinforcing the EU’s efforts to secure medicine supply chains.

The European Federation of Pharmaceutical Industries and Associations (EFPIA) welcomes the efforts to introduce criteria beyond price for the public procurement of critical medicines but raised concerns with the inclusion of strengthened collaborative procurement options. The options “may be appropriate under very specific circumstances where they accelerate patient access to critical medicines,” EFPIA said, but “a systematic application could create more harm than offering a more permanent solution to access related issues.” 

The trade group emphasized the need for clarity in identifying situations where collaborative procurement could enhance access beyond current national pricing and reimbursement systems.


Sources:

EC: Press corner

EC: Questions and answers on the Critical Medicines Act

EFPIA response to the Critical Medicines Act 


Meet the GMP Compliance Adviser

The GMP Compliance Adviser is the world's largest knowledge portal for quality management in the pharma business. 

The demo access is non-binding and ends automatically.

Test it now for free

You may also be interested in the following articles:

How is First Air Verified and Monitored During Aseptic Process Qualification?

How is First Air Verified and Monitored During Aseptic Process Qualification?

Here's the answer:
Read more
Outsourced Activities in the GDP Environment Part I: Supplier Management

Outsourced Activities in the GDP Environment Part I: Supplier Management

Supplier management is the systematic management of a company´s relationship with its suppliers. It encompasses supplier qualification and customer audits as described in the following excerpt from GMP:KnowHow Pharmalogistics (GDP).

Read more
FDA: Draft Guidance on Assessing Container Closure Systems for Drugs and Biologics

FDA: Draft Guidance on Assessing Container Closure Systems for Drugs and Biologics

On 14 August 2026, the US Food and Drug Administration (FDA) announced the publication of a new draft guidance document entitled ‘Container Closure Systems for Human Drugs and Biological Products’.

Read more
FDA: New FDA Commissioner Dr. Heidi Overton

FDA: New FDA Commissioner Dr. Heidi Overton

President Donald Trump has named White House aide Heidi Overton to lead the US Food and Drug Administration (FDA). Overton will fill the position previously held by Marty Makary, who left the agency in May. This announcement was made on Trump's Truth Social account on 19 August. Her nomination is subject to confirmation by the Senate.

Read more
IPEC: Stability Guide for Excipients has been Updated

IPEC: Stability Guide for Excipients has been Updated

The IPEC Stability Guide for Pharmaceutical Excipients has been updated and is now available as version 3 (2026), as announced on the IPEC (International Pharmaceutical Excipients Council) website.

Read more
EU: “Forever Chemicals” in a Conflict of Interests

EU: “Forever Chemicals” in a Conflict of Interests

On 14 July 2026, the European Parliamentary Research Service (EPRS) published a comprehensive briefing on PFAS (per- and polyfluoroalkyl substances), also known as ‘forever chemicals’. The document is intended to serve as a technical basis for MEPs in their upcoming political decisions on PFAS regulation and summarises the current state of scientific knowledge, regulation and procedures.

Read more
Previous
Next