Daniel M. Email & Phone Number

As a Senior Consultant at confinis AG, I help life sciences companies achieve compliance and excellence in regulatory affairs and quality management. With over 25 years of experience in the medical device, pharma, and electronic manufacturing industry, I have a proven track record of leading and supporting successful projects in various markets and domains. My core competencies include EU MDR-certification, CE-marking, FDA regulations, CAPA, quality auditing, and computer system validation. I was one of the first quality managers to obtain the MDR-certification for a medical device company that used nano materials in its products. I also have a strong academic background, with a Ph.D. in Natural Sciences from ETH Zürich, and multiple certifications in regulatory affairs and quality management. My mission is to leverage my expertise and skills to help clients navigate the complex and evolving regulatory landscape and ensure the safety and quality of their products and services.