Skip to main content Skip to search Skip to main navigation
News: Europe

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.


What is the problem?

Due to their favourable physico-chemical properties, PFAS are valuable for countless applications and products – including in the pharmaceutical sector. On the other hand, they pose an enormous challenge to the environment and human health: PFAS are persistent and have been detected worldwide in soil, water, food, wildlife and humans. Given the extent of contamination and the limitations of technically complex and costly remediation, scientists and regulatory authorities regard preventing further environmental pollution – i.e. regulating PFAS at source – as the most sustainable option.


What solutions are being discussed?

Due to the vast number of PFAS, regulating each individual compound is not feasible. The EU Chemicals Strategy for Sustainability therefore proposes regulating PFAS as a group. The European Chemicals Agency is currently reviewing a draft restriction under the EU Regulation on the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), which covers around 10,000 compounds. This would, in principle, prohibit the manufacture, placing on the market and use of PFAS, but provides for transition periods and sector-specific exemptions for applications where no suitable alternatives are currently available.


What happens next?

The European Chemicals Agency is expected to submit its final opinion to the European Commission by the end of 2026. The European Parliament will examine the Commission’s draft restriction. The European Commission will then present a concrete regulatory proposal for further deliberation.

The EPRS briefing highlights the key conflict of objectives:

  • Reducing risks to the environment and health through far-reaching restrictions
  • Whilst safeguarding critical applications and taking strategic industrial sectors into account


Quelle:

EP: Per- and polyfluoroalkyl substances (PDF)

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:

Outsourced Activities in the GDP Environment Part II: Contractual Agreements

Outsourced Activities in the GDP Environment Part II: Contractual Agreements

When outsourcing GDP activities, there is a need for concrete delimitation of responsibilities between a client and a contractor. Read more about the goals and the contents of a quality agreement in the following excerpt from GMP:KnowHow Pharmalogistics (GDP).

Read more
Question of the Week | GMP-Verlag

What are the Benefits and Limitations of Passive Temperature-Controlled Containers for Drug Transport?

Here's the answer:
Read more
FDA: Adjustment of Nitrosamine Limits for Short-Term Use Medicines

FDA: Adjustment of Nitrosamine Limits for Short-Term Use Medicines

The FDA has updated its recommendations on Acceptable Intake (AI) limits for nitrosamine impurities. Under certain conditions, the Agency now accepts a Less-Than-Lifetime (LTL) adjustment of AI limits for medicinal products that are not intended for lifetime use. This also represents an alignment with the LTL concept of ICH M7(R2).
Read more
Swissmedic: SMS Registration Becomes Prerequisite for GMP Certificates

Swissmedic: SMS Registration Becomes Prerequisite for GMP Certificates

As of 15 November 2026, active substances must be registered in the EMA's Substance Management Services (SMS) database before Swissmedic can include them in establishment licences and GMP certificates for active substance manufacturers. The new requirement results from modifications to the EudraGMDP database.
Read more
News: EMA

EMA: New Q&As for Biological Medicinal Products

The EMA has added a new section to its Q&As on biological medicinal products addressing medicinal products containing secretomes or extracellular vesicles (EVs) obtained from human or animal cells.
Read more
News: Europe

EU: Council Adopts the Pharmaceutical Package

On 28 September 2026, the Council of the European Union adopted the EU pharmaceutical package, marking another important step in the legislative process for the comprehensive reform of EU pharmaceutical legislation.
Read more
Previous
Next