AI and Automation for Regulatory Compliance in Medical Devices – Smarter Data Management

In today’s stringent regulatory environment, medical device and IVD manufacturers face mounting challenges to remain compliant while managing growing data complexities. Discover how AI and automation, including Celegence’s CAPTIS® platform, can streamline regulatory processes, improve data accuracy, and reduce compliance costs.

This on-demand webinar provides an in-depth overview of technology-driven solutions to help regulatory professionals modernize their compliance efforts. As regulatory demands evolve, smarter solutions like CAPTIS® are essential for managing compliance effectively.

The session demonstrates how AI-powered tools and automation technologies can simplify regulatory data management, optimize submission quality, and ensure compliance with EU MDR and IVDR requirements. By leveraging AI-driven solutions, regulatory teams can significantly ease their burden, improve efficiency, and drive precision in clinical and technical documentation processes.

With real-world insights and practical examples, this webinar equips you with actionable strategies to simplify regulatory affairs, enhance accuracy, and achieve cost-effective compliance management.

Don’t miss this opportunity to enhance your regulatory skills and understanding.

Webinar Speakers

  • Shruti Sharma: Product Specialist, CAPTIS® –  Celegence

  • Joseph Richardson Larbi: Director & Medical Device SME, Celegence

Gain actionable knowledge and insights with our webinar:

  • Simplify Dossier Management: Discover how AI tools streamline the creation and population of technical and clinical dossiers.

  • Improve Efficiency and Accuracy: Learn how automation reduces manual efforts and ensures data precision.

  • Meet Regulatory Expectations: Understand best practices to align with EU MDR and IVDR compliance standards.
  • Save Time and Costs: Explore how technology-driven solutions optimize resources and reduce compliance costs.
  • Enable Faster Decisions: See how AI accelerates decision-making for submissions and ongoing compliance.
Are you seeking assistance with a regulatory compliance need?

Please complete the form below to outline your medical device regulatory support requirements. Our team will promptly review your submission and reach out to confirm a consultation time. Thank you for your interest.