With over 25 years in the medical device industry 🏥, Elisabeth Sadka, M.Sc., MBA, leads HaMaDa Consulting’s Regulatory Affairs (RA), Quality Assurance (QA), and Clinical Writing teams. Her multidisciplinary expertise spans product development 🛠️, international regulatory affairs 🌍, quality management system implementation 📋, and clinical management 🩺.
Elisabeth brings a dynamic approach 💡 to navigating challenges and driving success. Under her leadership, HaMaDa Consulting ensures that medical device companies receive comprehensive services, guiding them through the complex regulatory landscape to achieve successful market entry 📈 and sustainability 🌱.
For more information on how Elisabeth and her team can support your medical device projects, visit HaMaDa Consulting’s website. 🌐
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