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As the year closes, this special podcast episode offers a comprehensive overview of what happened at Easy Medical Device in 2025 and the key priorities shaping 2026.
The episode reflects on a full year of continuous content creation, including:
- Weekly podcast episodes covering global medical device regulations
- Increased focus on artificial intelligence and its impact on QA/RA roles
- Educational initiatives such as EMD Mag, designed to make complex regulatory topics more accessible
- Development of digital tools like EasyIFU, labeling automation, and eQMS solutions
- Expansion of consulting, back-office services, and international presence
The discussion also addresses upcoming challenges:
- Increasing pressure on Notified Bodies
- Risks for late MDR/IVDR transitions
- The importance of anticipation and regulatory strategy for new and existing manufacturers
More than a recap, this episode is a strategic pause — an opportunity to reflect, learn, and prepare for the years ahead in a rapidly evolving medtech regulatory environment.
Who is Monir El Azzouzi?
Monir El Azzouzi is a Medical Device Expert specializing in Quality and Regulatory Affairs. After working for many years with big Healthcare companies, particularly Johnson and Johnson, he decided to create EasyMedicalDevice.com to help people better understand Medical Device Regulations worldwide. He has now created the consulting firm Easy Medical Device GmbH and developed many ways to deliver knowledge through videos, podcasts, online courses… His company also acts as Authorized Representative for the EU, UK, and Switzerland. Easy Medical Device becomes a one-stop shop for medical device manufacturers that need support on Quality and Regulatory Affairs.
Social Media to follow
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