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Overview What You Will Learn Webinar Speakers Who Should Watch?

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.

 

Where

Online Webinar

When

March 12, 2025 | 10:00 AM ET

Webinar Speakers

Director & Medical Device SME, Celegence

Joseph Richardson Larbi

Joseph has 20 years experience in medical device life cycle management and quality management systems (certified to ISO 13485, ISO 9001 & ISO/IEC17025). Key experience includes preparation and maintenance of technical files, product safety and vigilance reporting, clinical evaluations, risk assessment, regulatory audits, CE and notified body opinion submissions. Joseph has worked on diabetes management devices, nicotine replacement therapy (NRT) devices and pressurized metered dose inhalers (pMDI); Joseph has worked for small, medium and large Biotech companies such as Roche, OBG Pharmaceuticals and Kind Consumer Ltd.

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.