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Staying compliant with the EU Medical Device Regulation (MDR) is no longer just a checkbox exercise. As regulatory demands grow in complexity, medical device manufacturers must rethink their approach to compliance—prioritizing strategy, accuracy, and adaptability.
In this on-demand webinar, regulatory experts from Celegence provide a deep dive into the most pressing MDR challenges and how leading organizations are leveraging tools, processes, and expert insights to minimize risks and maintain certification with confidence.
Online Webinar
March 12, 2025 | 10:00 AM ET
Manager, Medical Device Services, Celegence
With 13 years in Life Sciences and over 5 years in medical device regulatory writing, Dr. Singh brings deep expertise in EU MDR clinical evaluation, PMS, and evidence development strategy.
Manager, Medical Device Services, Celegence
A regulatory specialist with 8+ years of experience, Dr. Chattopadhyaya has led EU MDR compliance initiatives across various device classes and therapeutic areas including orthopedic, ophthalmic, and emergency devices.
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