Kartik Patel is the Director of Quality Assurance and Regulatory Affairs at Bravida Medical. Kartik has successfully led various regulatory and compliance initiatives, including achieving CE compliance and managing the transition from EU MDD to EU MDR for a Class III combinational device. Kartik has also played a key role in the acquisition and integration of several companies and product portfolios. With a background in Medicinal and Pharmaceutical Chemistry, Nuclear Medicine Manufacturing, and Pharmacy, Kartik brings a wealth of expertise to their role in the healthcare industry.
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