Kamelija Milosev

Subject Matter Expert for Chemicals

 

Specialist subjects

EU chemicals | Biocides | Medical device legislation

 

Contribution types

Speaker | Content

 

Connect with Kamelija on LinkedIn

Kamelija Milosev is a Subject Matter Expert specializing in EU chemicals, biocides, and medical device legislation. She’s been with Enhesa since 2019 and has obtained her European Law Bachelors degree from the University of Maastricht and her Master of Law degree in Innovation, Technology and the Law from the University of Edinburgh, where she found herself most interested in the topics of bioethics and medical technology law.

Within the professional realm, Kamelija’s main areas of expertise pertain to the EU MDR, REACH, CLP, and BPR. She regularly guides organizations through these complex compliance landscapes, be it through personalized impact consultations, topic-specific trainings, articles, trend reports, or conference events. She also enjoys collaborating with other industry professionals and regulatory bodies on the aforementioned topics, and is a general fan of any collaborative effort that may result in deepening her regulatory knowledge.

Through a combination of legal acumen, practical experience and common sense, Kamelija helps organizations achieve regulatory compliance while mitigating potential risks in the fast-evolving EU legislative landscape of chemicals, biocides and medical devices.

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From this expert

Regulatory content and sustainability intelligence

PFAS in operations: EU regulatory trends for manufacturers

Detailing the presence and impact of PFAS across industries, and EU legislative restrictions to mitigate the substance.

Regulatory content and sustainability intelligence

The overlooked influence of women in environmental advocacy

In recognition of IDWGS, take a look back at the influential women in science who’ve had a lasting impact on environmental advocacy.

Regulatory content and sustainability intelligence

Introduction to the EU Medical Devices Framework

Embark on a comprehensive journey into the complex world of the EU Medical Devices Regulation (MDR) with our introductory training course.

Regulatory content and sustainability intelligence

PFAS: Global regulations, restrictions, and alternatives

Presenting PFAS in your operations: Key considerations and legislative updates for manufacturers

Regulatory content and sustainability intelligence

Regulatory Summit Europe, part 1: European updates

Presenting CLP revision: Adoption, implementation, and industry considerations

Regulatory content and sustainability intelligence

PFAS in your operations: Legislative trends for manufacturers

An industry-based overview of the latest regulations addressing PFAS emissions originating from manufacturing processes, and why reducing them matters.

Regulatory content and sustainability intelligence

Chemical safety data sheets

Clear on what’s compliant? The 2023 EU Enforcement Forum might make your business take a closer look at what you’re including on your safety data sheets.

Regulatory content and sustainability intelligence

How manufacturers need to adapt to changing PFAS regulations

Manufacturing Dive feature on why companies need to take notice of new regulations against forever chemicals, and how they can prepare to limit the substances in processes.

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