Name: Mr. Monir EL Azzouzi
Country: Switzerland
Qualification: Master’s in Quality and Performance Management
Designation: Founder & CEO
Company Name: Easy Medical Device.
Description:
Mr. Monir EL Azzouzi was Connected with International Fovea-Z Biomedical since July. Mr. Monir EL Azzouzi is a prominent figure in the field of Quality and Regulatory Affairs, currently serving as the Founder and CEO of Easy Medical Device based in Switzerland. With a Master's degree in Quality and Performance Management, Monir is dedicated to helping pharmaceutical and medical device companies navigate the complexities of regulatory compliance to ensure that patients receive safe and effective products. His extensive expertise encompasses Quality and Regulatory Affairs for medical devices and medicinal products, allowing him to provide invaluable guidance to organizations aiming to enhance their compliance and quality standards.
Recognizing a gap in accessible information regarding medical device regulations, Monir founded EasyMedicalDevice.com, a platform designed to simplify the often-complex landscape of medical device regulations and standards. Through this initiative, he empowers companies to better understand and meet their regulatory obligations. Monir actively engages with the community through multiple channels, including a blog, a YouTube channel, and a podcast titled "Medical Device Made Easy," which serve as vital resources for professionals in the medical device sector, offering insights and practical advice on successfully bringing compliant medical devices to market.
Guided by the principle, “Would I give this product to a member of my family?”, Monir’s commitment to patient safety drives every aspect of his work. He believes that every medical device should meet the highest safety and efficacy standards before reaching healthcare providers and patients. His specializations include Quality and Regulatory Affairs for medical devices, medicinal products, and combination products, along with a deep understanding of relevant regulations, such as the MDR 2017/745, IVDR 2017/746, FDA 21 CFR 820, and various ISO standards.
In addition, Monir is skilled in implementing process improvements, employing methodologies such as Change Management, PDCA (Plan-Do-Check-Act), and CAPA (Corrective and Preventive Actions) to enhance compliance and quality within organizations. Since his connection within the industry began in July, Monir has made significant contributions to advancing standards and practices in healthcare through Easy Medical Device, ensuring that medical devices meet rigorous safety and quality standards while enhancing the overall understanding of regulatory compliance among industry professional
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