Strengthened Environmental Risk Assessment requirements under the proposed new directive on medicinal products for human use
Written By
Senior Associate
Netherlands
As a senior associate in our Intellectual Property Group in Amsterdam, I specialise in life sciences patent law and life sciences regulatory.
Associate
Netherlands
As an associate in our Intellectual Property Group in The Hague, I offer our clients an all-round IP practice.
Legal Director
UK
I work as a Legal Director in London. As a member of our International Life Sciences Group, I specialise in European regulatory law concerning medicinal products, medical devices and related areas.
Related
Practices
Sectors
Regions
As part of the revision of the EU pharmaceutical legislative framework, a new directive on medicinal products for human use is proposed, which will repeal Directive 2001/83/EC. One of the objectives of this proposed directive is to reduce the environmental impact of medicinal products. This proposal strengthens the requirements for the environmental risk assessment (ERA) and extends the scope of the ERA to cover new protection goals, including antimicrobial resistance.
Currently, Article 8(3)(g) of Directive 2001/83/EC only requires an ERA to be submitted with the application for a marketing authorisation. The accompanying guidelines for the ERA describe how to assess the potential risks of the medicinal product to the environment and prescribe precautionary and safety measures to be considered if environmental risks cannot be excluded. However, under Directive 2001/83/EC, the result of the ERA cannot be a reason to refuse the marketing authorisation.
Latest insights
More Insights
ACMA Cracks Down on Non-Compliance with National Self-Exclusion Register Requirements
5 minutes Jun 04 2025
Latest developments in EU and German defence procurement: Defence procurement panel overview and key takeaways
5 minutes Jun 04 2025
Latest developments in UK and NATO DIANA defence procurement: Defence procurement panel overview and key takeaways
7 minutes Jun 04 2025