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Updated: Jun 23, 2026

Implementation of Portable Emissions Measurement Systems (PEMS) for the Real-driving Emissions (RDE) Regulation in Europe
09:34

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Published on: December 4, 2016

Addressing Eeuropean environmental legislation.

Maria Donawa1

  • 1Donawa Consulting, Rome, Italy. medonawa@donawa.com

Medical Device Technology
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PubMed
Summary
This summary is machine-generated.

European environmental regulations for medical device companies are now in effect. This article outlines key regulations and strategies for compliance to meet environmental protection standards.

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Area of Science:

  • Environmental Science
  • Regulatory Affairs

Background:

  • Medical device companies face evolving European environmental regulations.
  • Compliance deadlines for certain environmental requirements have already passed.

Purpose of the Study:

  • To discuss key European environmental regulations impacting medical device companies.
  • To present effective strategies for meeting these environmental requirements.

Main Methods:

  • Review of European Regulation (EU) XXXX/XXXX.
  • Analysis of Directive 2008/98/EC on waste.
  • Examination of Directive 2011/65/EU on RoHS.

Main Results:

  • Companies must adapt to new environmental compliance obligations.
  • Proactive environmental management is crucial for the medical device sector.

Conclusions:

  • Effective strategies are available for medical device companies to achieve environmental compliance.
  • Timely adherence to European environmental directives is essential.