Medical devices – how to navigate the role of importer or distributor

Medical devices – the path to CE marking and market
February 8, 2026
Medical devices – the path to CE marking and market
February 8, 2026
Medical devices must, in most cases, be CE marked before they can be used or sold in the EU/EEA. This course provides a clear and practical guide to the CE marking journey and market access. Learn what CE marking means, why it is required, and how the process works in practice.  The video explains conformity assessment, declaration of conformity, and key regulatory terms. Gain an overview of applicable regulations, including MDR and IVDR for medical devices.
 
Understand possible exceptions and when “research use only” may apply. See real examples of CE marking timelines and common regulatory pitfalls. Learn what to consider when developing, modifying, or adapting medical devices. The course also covers commercialization of research results.
 
Expert speakers share insights from startups to global medical device companies. Ideal for manufacturers, researchers, and professionals in medical technology
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Medical Device Mapping

Our Regulatory Affairs Services offer precise Medical Device Mapping solutions for navigating life science and health tech regulations. We ensure compliance with global requirements by assessing device classification, intended use, and regulatory status across markets. With our expertise, we streamline processes, mitigate risks, and accelerate time-to-market, empowering your organization to confidently navigate regulatory challenges.

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Regulatory Strategy

Our Regulatory Strategy services offer expert guidance through the complex regulations of life science and health tech. We collaborate closely with clients to develop aligned strategic plans, leveraging global regulatory expertise to optimize pathways for approval, market access, and compliance. From initial development to post-market needs, our meticulous approach ensures proactive compliance and sustainable growth.

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Regulatory Compliance

 
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Quality Management System

At Yallow, our Regulatory Affairs Services provide tailored Quality Management System (QMS) solutions for product safety, efficacy, and compliance in life science and health tech. We streamline processes to meet global standards and industry best practices, guiding you through documentation, training, risk management, and continuous improvement. With our QMS expertise, navigate regulations confidently, driving innovation in healthcare.

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Gap Analysis

At Yallow, our Regulatory Affairs Services offer thorough Gap Analysis expertise to pinpoint discrepancies between current practices and regulatory requirements in life science and health tech. With meticulous assessment and analysis, we provide actionable recommendations to ensure compliance with global regulations and industry standards, empowering organizations to proactively mitigate risks and maintain a competitive edge.

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Harmonized Standards

Harmonized standards are crucial for global trade and product safety, particularly in life science and health tech. At Yallow, we provide expert guidance on implementing these standards to streamline compliance and foster innovation. Our Regulatory Affairs Services ensure seamless alignment with requirements, enabling enhanced market access and consumer confidence. Trust us to navigate the complexities of harmonized standards, driving global progress.

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Audits

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UDI Implementation

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Risk Management