Artificial Intelligence is reshaping the world of Quality and Regulatory Affairs.

We discuss:

The reality behind “AI replacing QA/RA jobs”

Key tools: n8n, Make, Zapier, OpenAI, and OpenFDA

Building automation workflows for regulatory monitoring and documentation

Managing data privacy, confidentiality, and local vs cloud solutions

The cost, setup time, and risks of AI hallucination

How to use AI safely and ethically in regulated environments

👉 By the end, you’ll know how to build smart workflows that save time, ensure compliance, and keep human oversight where it matters most.

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

Monir El Azzouzi Linkedin: https://linkedin.com/in/melazzouzi

Twitter: https://twitter.com/elazzouzim

Pinterest: https://www.pinterest.com/easymedicaldevice

Instagram: https://www.instagram.com/easymedicaldevice