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Watch Now: Staying Compliant: Strategies for EU MDR and Beyond

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.

 

Where

Online Webinar

When

March 12, 2025 | 10:00 AM ET

What You Will Learn

  • ✔ How to reduce the burden of regional regulatory divergence and its impact on operational efficiency
  • ✔ Tools and technologies that improve the accuracy, consistency, and scalability of technical documentation
  • ✔ Best practices for creating audit-ready clinical evaluation deliverables under MDR
  • ✔ Regulatory updates you should act on now to stay aligned and ready for what’s ahead

Webinar Speakers

Manager, Medical Device Services, Celegence

Dr. Anushree Singh

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

Dr. Ipshita Chattopadhyaya

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.

Who Should Watch?

  • Regulatory Affairs and Quality Assurance professionals
  • Clinical Evaluation and Technical Documentation teams
  • Compliance and Risk Management leads
  • Medical device manufacturers supporting Class I–III products

Whether you’re preparing for your next audit or trying to streamline compliance processes, this webinar delivers relevant, real-world insights from experts who actively support global medical device firms.

Authored By

Shilpam Rajput

More by Shilpam Rajput